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dbSNP Short Genetic Variations

Welcome to the Reference SNP (rs) Report

All alleles are reported in the Forward orientation. Click on the Variant Details tab for details on Genomic Placement, Gene, and Amino Acid changes. HGVS names are in the HGVS tab.

Reference SNP (rs) Report

This page reports data for a single dbSNP Reference SNP variation (RefSNP or rs) from the new redesigned dbSNP build.
Top of the page reports a concise summary for the rs, with more specific details included in the corresponding tabs below.
All alleles are reported in the Forward orientation. Use the Genomic View to inspect the nucleotides flanking the variant, and its neighbors.
For more information see Help documentation.

rs10910733

Current Build 156

Released September 21, 2022

Organism
Homo sapiens
Position
chr1:148813084 (GRCh38.p14) Help

The anchor position for this RefSNP. Includes all nucleotides potentially affected by this change, thus it can differ from HGVS, which is right-shifted. See here for details.

Alleles
T>C
Variation Type
SNV Single Nucleotide Variation
Frequency
C=0.20632 (10557/51168, GnomAD)
C=0.05387 (1410/26174, 14KJPN)
C=0.11432 (1916/16760, 8.3KJPN) (+ 9 more)
C=0.10905 (1781/16332, ALFA)
C=0.1512 (968/6404, 1000G_30x)
C=0.1181 (345/2922, KOREAN)
C=0.0758 (123/1622, Korea1K)
C=0.052 (10/194, HapMap)
T=0.500 (61/122, SGDP_PRJ)
C=0.500 (61/122, SGDP_PRJ)
T=0.5 (3/6, Siberian)
C=0.5 (3/6, Siberian)
Clinical Significance
Not Reported in ClinVar
Gene : Consequence
PDE4DIP : Intron Variant
Publications
0 citations
Genomic View
See rs on genome

ALFA Allele Frequency
The ALFA project provide aggregate allele frequency from dbGaP. More information is available on the project page including descriptions, data access, and terms of use.

Release Version: 20230706150541
Population Group Sample Size Ref Allele Alt Allele
Total Global 16332 T=0.89095 C=0.10905
European Sub 12080 T=0.93369 C=0.06631
African Sub 2816 T=0.7486 C=0.2514
African Others Sub 108 T=0.704 C=0.296
African American Sub 2708 T=0.7504 C=0.2496
Asian Sub 108 T=0.917 C=0.083
East Asian Sub 84 T=0.90 C=0.10
Other Asian Sub 24 T=0.96 C=0.04
Latin American 1 Sub 146 T=0.801 C=0.199
Latin American 2 Sub 610 T=0.764 C=0.236
South Asian Sub 94 T=0.96 C=0.04
Other Sub 478 T=0.820 C=0.180


Help

Frequency tab displays a table of the reference and alternate allele frequencies reported by various studies and populations. Table lines, where Population="Global" refer to the entire study population, whereas lines, where Group="Sub", refer to a study-specific population subgroupings (i.e. AFR, CAU, etc.), if available. Frequency for the alternate allele (Alt Allele) is a ratio of samples observed-to-total, where the numerator (observed samples) is the number of chromosomes in the study with the minor allele present (found in "Sample size", where Group="Sub"), and the denominator (total samples) is the total number of all chromosomes in the study for the variant (found in "Sample size", where Group="Study-wide" and Population="Global").

Download
Study Population Group Sample Size Ref Allele Alt Allele
gnomAD - Genomes Global Study-wide 51168 T=0.79368 C=0.20632
gnomAD - Genomes European Sub 24680 T=0.87480 C=0.12520
gnomAD - Genomes African Sub 18688 T=0.70195 C=0.29805
gnomAD - Genomes American Sub 4640 T=0.7131 C=0.2869
gnomAD - Genomes Ashkenazi Jewish Sub 1386 T=0.7843 C=0.2157
gnomAD - Genomes East Asian Sub 1014 T=0.9063 C=0.0937
gnomAD - Genomes Other Sub 760 T=0.774 C=0.226
14KJPN JAPANESE Study-wide 26174 T=0.94613 C=0.05387
8.3KJPN JAPANESE Study-wide 16760 T=0.88568 C=0.11432
Allele Frequency Aggregator Total Global 16332 T=0.89095 C=0.10905
Allele Frequency Aggregator European Sub 12080 T=0.93369 C=0.06631
Allele Frequency Aggregator African Sub 2816 T=0.7486 C=0.2514
Allele Frequency Aggregator Latin American 2 Sub 610 T=0.764 C=0.236
Allele Frequency Aggregator Other Sub 478 T=0.820 C=0.180
Allele Frequency Aggregator Latin American 1 Sub 146 T=0.801 C=0.199
Allele Frequency Aggregator Asian Sub 108 T=0.917 C=0.083
Allele Frequency Aggregator South Asian Sub 94 T=0.96 C=0.04
1000Genomes_30x Global Study-wide 6404 T=0.8488 C=0.1512
1000Genomes_30x African Sub 1786 T=0.7307 C=0.2693
1000Genomes_30x Europe Sub 1266 T=0.9289 C=0.0711
1000Genomes_30x South Asian Sub 1202 T=0.8902 C=0.1098
1000Genomes_30x East Asian Sub 1170 T=0.9248 C=0.0752
1000Genomes_30x American Sub 980 T=0.819 C=0.181
KOREAN population from KRGDB KOREAN Study-wide 2922 T=0.8819 C=0.1181
Korean Genome Project KOREAN Study-wide 1622 T=0.9242 C=0.0758
HapMap Global Study-wide 194 T=0.948 C=0.052
HapMap American Sub 114 T=0.956 C=0.044
HapMap Asian Sub 80 T=0.94 C=0.06
SGDP_PRJ Global Study-wide 122 T=0.500 C=0.500
Siberian Global Study-wide 6 T=0.5 C=0.5
Help

Variant Details tab shows known variant placements on genomic sequences: chromosomes (NC_), RefSeqGene, pseudogenes or genomic regions (NG_), and in a separate table: on transcripts (NM_) and protein sequences (NP_). The corresponding transcript and protein locations are listed in adjacent lines, along with molecular consequences from Sequence Ontology. When no protein placement is available, only the transcript is listed. Column "Codon[Amino acid]" shows the actual base change in the format of "Reference > Alternate" allele, including the nucleotide codon change in transcripts, and the amino acid change in proteins, respectively, allowing for known ribosomal slippage sites. To view nucleotides adjacent to the variant use the Genomic View at the bottom of the page - zoom into the sequence until the nucleotides around the variant become visible.

Genomic Placements
Sequence name Change
GRCh38.p14 chr 1 NC_000001.11:g.148813084T>C
GRCh37.p13 chr 1 fix patch HG1287_PATCH NW_003871055.3:g.5628497T>C
PDE4DIP RefSeqGene NG_027693.2:g.9909T>C
GRCh37.p13 chr 1 NC_000001.10:g.145071307A>G
Gene: PDE4DIP, phosphodiesterase 4D interacting protein (plus strand)
Molecule type Change Amino acid[Codon] SO Term
PDE4DIP transcript variant 11 NM_001350521.4:c.233+4347…

NM_001350521.4:c.233+4347T>C

N/A Intron Variant
PDE4DIP transcript variant 14 NM_001377392.2:c.233+4347…

NM_001377392.2:c.233+4347T>C

N/A Intron Variant
PDE4DIP transcript variant 17 NM_001395298.1:c.233+4347…

NM_001395298.1:c.233+4347T>C

N/A Intron Variant
PDE4DIP transcript variant 19 NM_001395300.1:c.233+4347…

NM_001395300.1:c.233+4347T>C

N/A Intron Variant
PDE4DIP transcript variant 21 NM_001395302.1:c.233+4347…

NM_001395302.1:c.233+4347T>C

N/A Intron Variant
PDE4DIP transcript variant 22 NM_001395303.1:c.233+4347…

NM_001395303.1:c.233+4347T>C

N/A Intron Variant
PDE4DIP transcript variant 26 NM_001395307.1:c.233+4347…

NM_001395307.1:c.233+4347T>C

N/A Intron Variant
PDE4DIP transcript variant 35 NM_001395316.1:c.233+4347…

NM_001395316.1:c.233+4347T>C

N/A Intron Variant
PDE4DIP transcript variant 36 NM_001395317.1:c.233+4347…

NM_001395317.1:c.233+4347T>C

N/A Intron Variant
PDE4DIP transcript variant 38 NM_001395319.1:c.-29+4176…

NM_001395319.1:c.-29+4176T>C

N/A Intron Variant
PDE4DIP transcript variant 41 NM_001395322.1:c.-219+434…

NM_001395322.1:c.-219+4347T>C

N/A Intron Variant
PDE4DIP transcript variant 44 NM_001395325.1:c.233+4347…

NM_001395325.1:c.233+4347T>C

N/A Intron Variant
PDE4DIP transcript variant 47 NM_001395328.1:c.-367+434…

NM_001395328.1:c.-367+4347T>C

N/A Intron Variant
PDE4DIP transcript variant 48 NM_001395329.1:c.-394+434…

NM_001395329.1:c.-394+4347T>C

N/A Intron Variant
PDE4DIP transcript variant 3 NM_022359.8:c.233+4347T>C N/A Intron Variant
PDE4DIP transcript variant 4 NM_001002810.5:c. N/A Genic Upstream Transcript Variant
PDE4DIP transcript variant 5 NM_001002811.3:c. N/A Genic Upstream Transcript Variant
PDE4DIP transcript variant 2 NM_001002812.4:c. N/A Genic Upstream Transcript Variant
PDE4DIP transcript variant 6 NM_001195260.2:c. N/A Genic Upstream Transcript Variant
PDE4DIP transcript variant 7 NM_001195261.2:c. N/A Genic Upstream Transcript Variant
PDE4DIP transcript variant 8 NM_001198832.4:c. N/A Genic Upstream Transcript Variant
PDE4DIP transcript variant 9 NM_001198834.5:c. N/A Genic Upstream Transcript Variant
PDE4DIP transcript variant 10 NM_001350520.2:c. N/A Genic Upstream Transcript Variant
PDE4DIP transcript variant 12 NM_001350522.3:c. N/A Genic Upstream Transcript Variant
PDE4DIP transcript variant 13 NM_001350523.3:c. N/A Genic Upstream Transcript Variant
PDE4DIP transcript variant 15 NM_001377393.2:c. N/A Genic Upstream Transcript Variant
PDE4DIP transcript variant 16 NM_001395297.1:c. N/A Genic Upstream Transcript Variant
PDE4DIP transcript variant 18 NM_001395299.1:c. N/A Genic Upstream Transcript Variant
PDE4DIP transcript variant 20 NM_001395301.1:c. N/A Genic Upstream Transcript Variant
PDE4DIP transcript variant 23 NM_001395304.1:c. N/A Genic Upstream Transcript Variant
PDE4DIP transcript variant 24 NM_001395305.1:c. N/A Genic Upstream Transcript Variant
PDE4DIP transcript variant 25 NM_001395306.1:c. N/A Genic Upstream Transcript Variant
PDE4DIP transcript variant 27 NM_001395308.1:c. N/A Genic Upstream Transcript Variant
PDE4DIP transcript variant 28 NM_001395309.1:c. N/A Genic Upstream Transcript Variant
PDE4DIP transcript variant 29 NM_001395310.1:c. N/A Genic Upstream Transcript Variant
PDE4DIP transcript variant 30 NM_001395311.1:c. N/A Genic Upstream Transcript Variant
PDE4DIP transcript variant 31 NM_001395312.1:c. N/A Genic Upstream Transcript Variant
PDE4DIP transcript variant 32 NM_001395313.1:c. N/A Genic Upstream Transcript Variant
PDE4DIP transcript variant 33 NM_001395314.1:c. N/A Genic Upstream Transcript Variant
PDE4DIP transcript variant 34 NM_001395315.1:c. N/A Genic Upstream Transcript Variant
PDE4DIP transcript variant 37 NM_001395318.1:c. N/A Genic Upstream Transcript Variant
PDE4DIP transcript variant 39 NM_001395320.1:c. N/A Genic Upstream Transcript Variant
PDE4DIP transcript variant 40 NM_001395321.1:c. N/A Genic Upstream Transcript Variant
PDE4DIP transcript variant 42 NM_001395323.1:c. N/A Genic Upstream Transcript Variant
PDE4DIP transcript variant 43 NM_001395324.1:c. N/A Genic Upstream Transcript Variant
PDE4DIP transcript variant 45 NM_001395326.1:c. N/A Genic Upstream Transcript Variant
PDE4DIP transcript variant 46 NM_001395327.1:c. N/A Genic Upstream Transcript Variant
PDE4DIP transcript variant 49 NM_001395426.1:c. N/A Genic Upstream Transcript Variant
PDE4DIP transcript variant 1 NM_014644.7:c. N/A Genic Upstream Transcript Variant
PDE4DIP transcript variant X23 XM_011510176.3:c.233+4347…

XM_011510176.3:c.233+4347T>C

N/A Intron Variant
PDE4DIP transcript variant X22 XM_024451068.2:c.233+4347…

XM_024451068.2:c.233+4347T>C

N/A Intron Variant
PDE4DIP transcript variant X6 XM_047435063.1:c.233+4347…

XM_047435063.1:c.233+4347T>C

N/A Intron Variant
PDE4DIP transcript variant X8 XM_047435064.1:c.233+4347…

XM_047435064.1:c.233+4347T>C

N/A Intron Variant
PDE4DIP transcript variant X9 XM_047435065.1:c.233+4347…

XM_047435065.1:c.233+4347T>C

N/A Intron Variant
PDE4DIP transcript variant X12 XM_047435066.1:c.233+4347…

XM_047435066.1:c.233+4347T>C

N/A Intron Variant
PDE4DIP transcript variant X14 XM_047435070.1:c.233+4347…

XM_047435070.1:c.233+4347T>C

N/A Intron Variant
PDE4DIP transcript variant X17 XM_047435071.1:c.233+4347…

XM_047435071.1:c.233+4347T>C

N/A Intron Variant
PDE4DIP transcript variant X21 XM_047435075.1:c.233+4347…

XM_047435075.1:c.233+4347T>C

N/A Intron Variant
PDE4DIP transcript variant X24 XM_047435076.1:c.233+4347…

XM_047435076.1:c.233+4347T>C

N/A Intron Variant
PDE4DIP transcript variant X1 XM_005272981.4:c. N/A Genic Upstream Transcript Variant
PDE4DIP transcript variant X2 XM_017002879.2:c. N/A Genic Upstream Transcript Variant
PDE4DIP transcript variant X3 XM_017002881.2:c. N/A Genic Upstream Transcript Variant
PDE4DIP transcript variant X4 XM_017002882.2:c. N/A Genic Upstream Transcript Variant
PDE4DIP transcript variant X5 XM_017002883.2:c. N/A Genic Upstream Transcript Variant
PDE4DIP transcript variant X7 XM_017002884.2:c. N/A Genic Upstream Transcript Variant
PDE4DIP transcript variant X10 XM_017002885.2:c. N/A Genic Upstream Transcript Variant
PDE4DIP transcript variant X11 XM_017002886.2:c. N/A Genic Upstream Transcript Variant
PDE4DIP transcript variant X13 XM_017002890.2:c. N/A Genic Upstream Transcript Variant
PDE4DIP transcript variant X15 XM_017002896.2:c. N/A Genic Upstream Transcript Variant
PDE4DIP transcript variant X16 XM_017002897.2:c. N/A Genic Upstream Transcript Variant
PDE4DIP transcript variant X25 XM_017002900.2:c. N/A Genic Upstream Transcript Variant
PDE4DIP transcript variant X26 XM_017002901.2:c. N/A Genic Upstream Transcript Variant
PDE4DIP transcript variant X18 XM_047435072.1:c. N/A Genic Upstream Transcript Variant
PDE4DIP transcript variant X19 XM_047435073.1:c. N/A Genic Upstream Transcript Variant
PDE4DIP transcript variant X20 XM_047435074.1:c. N/A Genic Upstream Transcript Variant
PDE4DIP transcript variant X27 XM_047435081.1:c. N/A Genic Upstream Transcript Variant
PDE4DIP transcript variant X28 XM_047435082.1:c. N/A Genic Upstream Transcript Variant
Help

Clinical Significance tab shows a list of clinical significance entries from ClinVar associated with the variation, per allele. Click on the RCV accession (i.e. RCV000001615.2) or Allele ID (i.e. 12274) to access full ClinVar report.

Not Reported in ClinVar
Help

Aliases tab displays HGVS names representing the variant placements and allele changes on genomic, transcript and protein sequences, per allele. HGVS name is an expression for reporting sequence accession and version, sequence type, position, and allele change. The column "Note" can have two values: "diff" means that there is a difference between the reference allele (variation interval) at the placement reported in HGVS name and the reference alleles reported in other HGVS names, and "rev" means that the sequence of this variation interval at the placement reported in HGVS name is in reverse orientation to the sequence(s) of this variation in other HGVS names not labeled as "rev".

Placement T= C
GRCh38.p14 chr 1 NC_000001.11:g.148813084= NC_000001.11:g.148813084T>C
GRCh37.p13 chr 1 fix patch HG1287_PATCH NW_003871055.3:g.5628497= NW_003871055.3:g.5628497T>C
PDE4DIP RefSeqGene NG_027693.2:g.9909= NG_027693.2:g.9909T>C
GRCh37.p13 chr 1 NC_000001.10:g.145071307= NC_000001.10:g.145071307A>G
PDE4DIP transcript variant 11 NM_001350521.4:c.233+4347= NM_001350521.4:c.233+4347T>C
PDE4DIP transcript variant 14 NM_001377392.2:c.233+4347= NM_001377392.2:c.233+4347T>C
PDE4DIP transcript variant 17 NM_001395298.1:c.233+4347= NM_001395298.1:c.233+4347T>C
PDE4DIP transcript variant 19 NM_001395300.1:c.233+4347= NM_001395300.1:c.233+4347T>C
PDE4DIP transcript variant 21 NM_001395302.1:c.233+4347= NM_001395302.1:c.233+4347T>C
PDE4DIP transcript variant 22 NM_001395303.1:c.233+4347= NM_001395303.1:c.233+4347T>C
PDE4DIP transcript variant 26 NM_001395307.1:c.233+4347= NM_001395307.1:c.233+4347T>C
PDE4DIP transcript variant 35 NM_001395316.1:c.233+4347= NM_001395316.1:c.233+4347T>C
PDE4DIP transcript variant 36 NM_001395317.1:c.233+4347= NM_001395317.1:c.233+4347T>C
PDE4DIP transcript variant 38 NM_001395319.1:c.-29+4176= NM_001395319.1:c.-29+4176T>C
PDE4DIP transcript variant 41 NM_001395322.1:c.-219+4347= NM_001395322.1:c.-219+4347T>C
PDE4DIP transcript variant 44 NM_001395325.1:c.233+4347= NM_001395325.1:c.233+4347T>C
PDE4DIP transcript variant 47 NM_001395328.1:c.-367+4347= NM_001395328.1:c.-367+4347T>C
PDE4DIP transcript variant 48 NM_001395329.1:c.-394+4347= NM_001395329.1:c.-394+4347T>C
PDE4DIP transcript variant 3 NM_022359.5:c.233+4323= NM_022359.5:c.233+4323T>C
PDE4DIP transcript variant 3 NM_022359.8:c.233+4347= NM_022359.8:c.233+4347T>C
PDE4DIP transcript variant X2 XM_005272982.1:c.233+4323= XM_005272982.1:c.233+4323T>C
PDE4DIP transcript variant X6 XM_005277447.1:c.233+4347= XM_005277447.1:c.233+4347T>C
PDE4DIP transcript variant X23 XM_011510176.3:c.233+4347= XM_011510176.3:c.233+4347T>C
PDE4DIP transcript variant X22 XM_024451068.2:c.233+4347= XM_024451068.2:c.233+4347T>C
PDE4DIP transcript variant X6 XM_047435063.1:c.233+4347= XM_047435063.1:c.233+4347T>C
PDE4DIP transcript variant X8 XM_047435064.1:c.233+4347= XM_047435064.1:c.233+4347T>C
PDE4DIP transcript variant X9 XM_047435065.1:c.233+4347= XM_047435065.1:c.233+4347T>C
PDE4DIP transcript variant X12 XM_047435066.1:c.233+4347= XM_047435066.1:c.233+4347T>C
PDE4DIP transcript variant X14 XM_047435070.1:c.233+4347= XM_047435070.1:c.233+4347T>C
PDE4DIP transcript variant X17 XM_047435071.1:c.233+4347= XM_047435071.1:c.233+4347T>C
PDE4DIP transcript variant X21 XM_047435075.1:c.233+4347= XM_047435075.1:c.233+4347T>C
PDE4DIP transcript variant X24 XM_047435076.1:c.233+4347= XM_047435076.1:c.233+4347T>C
Help

Submissions tab displays variations originally submitted to dbSNP, now supporting this RefSNP cluster (rs). We display Submitter handle, Submission identifier, Date and Build number, when the submission appeared for the first time. Direct submissions to dbSNP have Submission ID in the form of an ss-prefixed number (ss#). Other supporting variations are listed in the table without ss#.

23 SubSNP, 10 Frequency submissions
No Submitter Submission ID Date (Build)
1 SC_SNP ss18136139 Feb 27, 2004 (120)
2 SC_SNP ss18607164 Feb 27, 2004 (120)
3 COMPLETE_GENOMICS ss167080937 Jul 04, 2010 (132)
4 BL ss253463652 May 09, 2011 (134)
5 DDI ss1425962688 Apr 09, 2015 (144)
6 HAMMER_LAB ss1795028329 Sep 11, 2015 (146)
7 USC_VALOUEV ss2147971544 Oct 11, 2018 (152)
8 GRF ss2697930469 Oct 11, 2018 (152)
9 GNOMAD ss2760576698 Oct 11, 2018 (152)
10 SWEGEN ss2987632344 Oct 11, 2018 (152)
11 CSHL ss3343682151 Oct 11, 2018 (152)
12 EVA ss3746753285 Jul 12, 2019 (153)
13 PACBIO ss3783547248 Jul 12, 2019 (153)
14 PACBIO ss3794056591 Jul 12, 2019 (153)
15 SGDP_PRJ ss3849859956 Apr 25, 2020 (154)
16 KRGDB ss3895032472 Apr 25, 2020 (154)
17 KOGIC ss3945570920 Apr 25, 2020 (154)
18 GNOMAD ss4002962487 Apr 25, 2021 (155)
19 TOMMO_GENOMICS ss5146154401 Apr 25, 2021 (155)
20 EVA ss5321682700 Oct 17, 2022 (156)
21 1000G_HIGH_COVERAGE ss5517424552 Oct 17, 2022 (156)
22 TOMMO_GENOMICS ss5673426001 Oct 17, 2022 (156)
23 YY_MCH ss5801229005 Oct 17, 2022 (156)
24 1000Genomes_30x NC_000001.11 - 148813084 Oct 17, 2022 (156)
25 gnomAD - Genomes NC_000001.11 - 148813084 Apr 25, 2021 (155)
26 HapMap NC_000001.11 - 148813084 Apr 25, 2020 (154)
27 KOREAN population from KRGDB NC_000001.10 - 145071307 Apr 25, 2020 (154)
28 Korean Genome Project NC_000001.11 - 148813084 Apr 25, 2020 (154)
29 SGDP_PRJ NC_000001.10 - 145071307 Apr 25, 2020 (154)
30 Siberian NC_000001.10 - 145071307 Apr 25, 2020 (154)
31 8.3KJPN NC_000001.10 - 145071307 Apr 25, 2021 (155)
32 14KJPN NC_000001.11 - 148813084 Oct 17, 2022 (156)
33 ALFA NC_000001.11 - 148813084 Apr 25, 2021 (155)
Help

History tab displays RefSNPs (Associated ID) from previous builds (Build) that now support the current RefSNP, and the dates, when the history was updated for each Associated ID (History Updated).

Added to this RefSNP Cluster:
Submission IDs Observation SPDI Canonical SPDI Source RSIDs
ss167080937, ss253463652 NC_000001.9:143782663:A:G NC_000001.11:148813083:T:C (self)
2209866, 1876936, 487898, 4123708, ss1425962688, ss1795028329, ss2147971544, ss2697930469, ss2760576698, ss2987632344, ss3343682151, ss3746753285, ss3783547248, ss3794056591, ss3849859956, ss3895032472, ss5146154401, ss5321682700 NC_000001.10:145071306:A:G NC_000001.11:148813083:T:C (self)
4950487, 25943175, 170302, 1948921, 7263105, 9643314562, ss3945570920, ss4002962487, ss5517424552, ss5673426001, ss5801229005 NC_000001.11:148813083:T:C NC_000001.11:148813083:T:C (self)
ss18136139, ss18607164 NT_004434.16:260582:A:G NC_000001.11:148813083:T:C (self)
Help

Publications tab displays PubMed articles citing the variation as a listing of PMID, Title, Author, Year, Journal, ordered by Year, descending.

No publications for rs10910733

Help

The Flanks tab provides retrieving flanking sequences of a SNP on all molecules that have placements.

Genome context:
Select flank length:

Genomic regions, transcripts, and products
Top Help

NCBI Graphical Sequence Viewer display of the genomic region, transcripts and protein products for the reported RefSNP (rs).
Use the zoom option to view the nucleotides around the RefSNP and find other neighboring RefSNPs.
Visit Sequence Viewer for help with navigating inside the display and modifying the selection of displayed data tracks.

Software version is: 2.0.1.post761+d5e8e07