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rs864622263

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs864622263(G;G)
Make rs864622263(G;T)
ReferenceGRCh38.p2 38.2/147
Chromosome9
Position21974781
GeneCDKN2A
is asnp
is mentioned by
dbSNPrs864622263
ebirs864622263
HLIrs864622263
Exacrs864622263
Varsomers864622263
Maprs864622263
PheGenIrs864622263
hapmaprs864622263
1000 genomesrs864622263
hgdprs864622263
ensemblrs864622263
gopubmedrs864622263
geneviewrs864622263
scholarrs864622263
googlers864622263
pharmgkbrs864622263
gwascentralrs864622263
openSNPrs864622263
23andMers864622263
23andMe allrs864622263
SNP Nexus

SNPshotrs864622263
SNPdbers864622263
MSV3drs864622263
GWAS Ctlgrs864622263
Max Magnitude0
ClinVar
Risk rs864622263(G;G)
Alt rs864622263(G;G)
Reference rs864622263(T;T)
Significance Probable-Pathogenic
Disease Hereditary cutaneous melanoma not provided
Variation info
Gene CDKN2A
CLNDBN Hereditary cutaneous melanoma not provided
Reversed 1
HGVS NC_000009.11:g.21974780A>C
CLNSRC
CLNACC RCV000206427.1, RCV000235523.1,