Submitter | Handle | ILLUMINA | Submitter SNP ID | HumanOmniExpress-12v1_C_rs8176746-131_T_F_1858937746 | RefSNP(rs#) | rs8176746 | Submitted Batch ID | HumanOmniExpress-12v1_C | Submitted Date | Jan 30, 2012 | Publication Cited | N.D. | First entry to dbSNP | Jan 30 2012 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 | ILLUMINA-CHIP | Ascertainment Samplesize | 2 | Population | N.D. |
| Allele | Observed Allele | G/T | Ancestral Allele | N.D. | Allele Origin | N/A | SNP Class | SNV | CpG Code | N.D. |
| | Variation | Frequency Submission | N.D. | Genotype Summary | N.D. | Genotype Submission | N.D. | Haplotype | N.D. |
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>gnl|dbSNP|ss481827964|allelePos=26|len=51|taxid=9606|alleles='G/T'|mol=Genomic ACCGACCCCC CGAAGAACCC CCCCA
K
GTAGTAGAAA TCGCCCTCGT CCTTG
There is no frequency submission for ss481827964.
No sufficient data to compute Hardy-weinberg probability for ss481827964.
There is no individual genotype data for ss481827964.
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