Submitter | Handle | ILLUMINA | Submitter SNP ID | HumanOmniExpress-12v1_H_rs1000002-131_T_F_1856971897 | RefSNP(rs#) | rs1000002 | 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 | C/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|ss831884880|allelePos=26|len=51|taxid=9606|alleles='C/T'|mol=Genomic CAAGTACTAG CTCTGATGGT TCTCA
Y
TTGGACAGCA GCCAGCTTAG TCCTC
There is no frequency submission for ss831884880.
No sufficient data to compute Hardy-weinberg probability for ss831884880.
There is no individual genotype data for ss831884880.
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