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Select item 5161151.

rs516115 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C,G [Show Flanks]
Chromosome:: 12:91163515 (GRCh38)
12:91557292 (GRCh37)
Canonical SPDI:: NC_000012.12:91163514:T:C,NC_000012.12:91163514:T:G
Gene:: DCN (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0.298266/74721 (ALFA)
C=0.175/7 (GENOME_DK)
C=0.228333/137 (NorthernSweden)
C=0.234469/234 (GoNL)
C=0.260268/1166 (Estonian)
C=0.271845/1008 (TWINSUK)
C=0.28438/1096 (ALSPAC)
C=0.328704/71 (Qatari)
T=0.338235/115 (SGDP_PRJ)
C=0.365065/6118 (TOMMO)
C=0.384483/53813 (GnomAD)
C=0.388608/307 (PRJEB37584)
C=0.403072/1181 (KOREAN)
C=0.404794/107145 (TOPMED)
C=0.40566/86 (Vietnamese)
C=0.41599/2083 (1000Genomes)
T=0.416667/10 (Siberian)
C=0.463415/152 (HapMap)
C=0.47474/37362 (PAGE_STUDY)
HGVS:: NC_000012.12:g.91163515T>C, NC_000012.12:g.91163515T>G, NC_000012.11:g.91557292T>C, NC_000012.11:g.91557292T>G, NG_011672.1:g.24515A>G, NG_011672.1:g.24515A>C

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