Submitter | Handle | ILLUMINA | Submitter SNP ID | HumanOmni1-Quad_v1-0_C_rs1800863-131_B_F_1863275786 | RefSNP(rs#) | rs1800863 | Submitted Batch ID | HumanOmni1-Quad_v1-0_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 | C/G | Ancestral Allele | N.D. | Allele Origin | G:Germline C:Germline | 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|ss481067498|allelePos=26|len=51|taxid=9606|alleles='C/G'|mol=Genomic CCCGAGATGT TTATGAAGAG GATTC
S
TACGTGAAGA GGAGCCAGGT GCCCA
There is no frequency submission for ss481067498.
No sufficient data to compute Hardy-weinberg probability for ss481067498.
There is no individual genotype data for ss481067498.
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