Submitter | Handle | ILLUMINA | Submitter SNP ID | HumanOmniExpress-12v1_H_rs17036076-131_B_R_1858001061 | RefSNP(rs#) | rs17036076 | Submitted Batch ID | HumanOmniExpress-12v1_H | Submitted Date | Sep 17, 2013 | Publication Cited | N.D. | First entry to dbSNP | Sep 17 2013 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 | A/G | 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. |
|
>gnl|dbSNP|ss832138222|allelePos=26|len=51|taxid=9606|alleles='A/G'|mol=Genomic GAGAAGAAAA GCTGTTTAGA GCTTT
R
GAAAAGACTG TGAGGCTTTG TGTGA
There is no frequency submission for ss832138222.
No sufficient data to compute Hardy-weinberg probability for ss832138222.
There is no individual genotype data for ss832138222.
|