Submitter | Handle | CLINVAR | Submitter SNP ID | SCV000337555 | RefSNP(rs#) | rs397515332 | Submitted Batch ID | CLINVAR_2016-11-30 | Submitted Date | Dec 04, 2016 | Publication Cited | N.D. | First entry to dbSNP | Dec 4 2016 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 | Submitted HGVS | NC_000002.11:g.238269781C>G |
| Assay | Species | Homo sapiens | Molecular Type | genomic | Method | CLINICAL_SNP_SUBMISSION | Ascertainment Samplesize | N.D. | Population | N.D. |
| Allele | Observed Allele | C/G | Ancestral Allele | N.D. | Allele Origin | G:Germline 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|ss2136849438|allelePos=51|len=101|taxid=9606|alleles='C/G'|mol=Genomic GAAATTTTAG GGACTAAAAC AATTTTTACT TACGGGTCCA CCCTCATCAC
S
AGGATAGCCT CGGTAGCCGT CTTCTCCAGG AATACCCTGA AACAAAGTAA
There is no frequency submission for ss2136849438.
No sufficient data to compute Hardy-weinberg probability for ss2136849438.
There is no individual genotype data for ss2136849438.
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