| Submitter | | Handle | BIOINF_KMB_FNS_UNIBA | | Submitter SNP ID | 7.24994001A>G | | RefSNP(rs#) | rs181 | | 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 | A/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|ss3025960272|allelePos=26|len=51|taxid=9606|alleles='A/G'|mol=Genomic CATGATTTCA TTCTTTTCTT ATGGC
R
GCTTTGTATT CTGTGACGTA TATGT
There is no frequency submission for ss3025960272.
No sufficient data to compute Hardy-weinberg probability for ss3025960272.
There is no individual genotype data for ss3025960272.
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