Submitter | Handle | ILLUMINA | Submitter SNP ID | HumanOmni25Exome-8v1_A_exm699019-0_B_F_1922989737 | RefSNP(rs#) | rs76092830 | Submitted Batch ID | HumanOmni25Exome-8v1_A | Submitted Date | May 30, 2013 | Publication Cited | N.D. | First entry to dbSNP | May 30 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 | T/C | 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|ss780869704|allelePos=26|len=51|taxid=9606|alleles='T/C'|mol=Genomic AGAGTCTCAA TGCCATCATA TTCCA
Y
TGGATCCCAG CGCAATTTAT AATCA
There is no frequency submission for ss780869704.
No sufficient data to compute Hardy-weinberg probability for ss780869704.
There is no individual genotype data for ss780869704.
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