| Resource Links | GenBank Accession | NC_000001
| 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 | LOW_COVERAGE | Ascertainment Samplesize | 1258 | 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|ss329116276|allelePos=51|len=101|taxid=9606|alleles='C/G'|mol=Genomic CCTGGGAAGC GCAAGGGGTC AGGGAGTTCC CTTTCCGAGT CAAAGAAAGG
S
GTGACGGACG CACCTGGAAA ATTGGGTCAC TCCCACCCGA ATACTGCGCT
There is no frequency submission for ss329116276.
No sufficient data to compute Hardy-weinberg probability for ss329116276.
There is no individual genotype data for ss329116276.
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