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Select item 29790991.

rs2979099 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 8:144763017 (GRCh38)
8:145988402 (GRCh37)
Canonical SPDI:: NC_000008.11:144763016:C:T
Gene:: LOC107986986 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0./0 (HapMap)
T=0.000015/4 (TOPMED)
T=0.00002/3 (GnomAD_genomes)
HGVS:: NC_000008.11:g.144763017C>T, NC_000008.10:g.145988402C>T, NG_115619.1:g.1098C>T, XR_001746149.3:n.5886C>T, XR_001746150.3:n.5876C>T

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