Submitter | Handle | CLINVAR | Submitter SNP ID | SCV000167705 | RefSNP(rs#) | rs56344740 | Submitted Batch ID | CLINVAR_2014-11-21 | Submitted Date | Nov 23, 2014 | Publication Cited | N.D. | First entry to dbSNP | Nov 23 2014 12:00:00:000AM |
| Resource Links | Submitted Gene Name | CHRNA2 | Submitted Gene ID | N.D. | Submitted SNP Synonyms | N.D | Submitted linkout | N.D | Submitted HGVS | NG_015827.1:g.21288C>A |
| Assay | Species | Homo sapiens | Molecular Type | genomic | Method | CLINICAL_SNP_SUBMISSION | Ascertainment Samplesize | N.D. | Population | N.D. |
| Allele | Observed Allele | C/A | Ancestral Allele | N.D. | Allele Origin | A: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|ss1457616992|allelePos=51|len=101|taxid=9606|alleles='C/A'|mol=Genomic CTATCACCCC ACATGCAGAA GGCACTGGAA GGTGTGCACT ACATTGCCGA
M
CACCTGCGGT CTGAGGATGC TGACTCTTCG GTGCGTTGGG GTTGGGAGAG
There is no frequency submission for ss1457616992.
No sufficient data to compute Hardy-weinberg probability for ss1457616992.
There is no individual genotype data for ss1457616992.
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