Submitter | Handle | BIOINF_KMB_FNS_UNIBA | Submitter SNP ID | 22.42121985C>G | RefSNP(rs#) | rs6002626 | Submitted Batch ID | Horsa 1.0 | Submitted Date | Jul 05, 2017 | Publication Cited | [1] Non invasive prenatal testing is a valuable source of population specific allelic frequencies | First entry to dbSNP | Jul 5 2017 12:00:00:000AM |
| Resource Links | Submitted Gene Name | N.D | Submitted Gene ID | N.D. | Submitted SNP Synonyms | N.D | Submitted linkout | N.D |
| Assay | Species | Homo sapiens | Molecular Type | Genomic | Method | LOWCOVERAGENGS | Ascertainment Samplesize | 1548 | Population | N.D. |
| Allele | Observed Allele | C/G | Ancestral Allele | N.D. | Allele Origin | N/A | SNP Class | SNV | CpG Code | N.D. |
| Validation | Validation Status | Not Validated | HWE Goodness of Fit | not applicable | Homozygote Detected | | PCR Confirmed | | In Expressed Sequence | |
| Variation | Frequency Submission | N.D. | Genotype Summary | N.D. | Genotype Submission | N.D. | Haplotype | N.D. |
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>gnl|dbSNP|ss3028962562|allelePos=26|len=51|taxid=9606|alleles='C/G'|mol=Genomic CTTTGCAGTA CATTTAGACA GATCA
S
GTCATTTCTC CATATGATCA TTTTC
There is no frequency submission for ss3028962562.
No sufficient data to compute Hardy-weinberg probability for ss3028962562.
There is no individual genotype data for ss3028962562.
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