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rs786204195

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs786204195(A;A)
Make rs786204195(A;C)
ReferenceGRCh38.p2 38.2/146
Chromosome9
Position21974686
GeneCDKN2A
is asnp
is mentioned by
dbSNPrs786204195
ebirs786204195
HLIrs786204195
Exacrs786204195
Varsomers786204195
Maprs786204195
PheGenIrs786204195
hapmaprs786204195
1000 genomesrs786204195
hgdprs786204195
ensemblrs786204195
gopubmedrs786204195
geneviewrs786204195
scholarrs786204195
googlers786204195
pharmgkbrs786204195
gwascentralrs786204195
openSNPrs786204195
23andMers786204195
23andMe allrs786204195
SNP Nexus

SNPshotrs786204195
SNPdbers786204195
MSV3drs786204195
GWAS Ctlgrs786204195
Max Magnitude0
ClinVar
Risk rs786204195(A,T;A,T)
Alt rs786204195(A,T;A,T)
Reference rs786204195(C;C)
Significance Pathogenic
Disease Hereditary cutaneous melanoma
Variation info
Gene CDKN2A
CLNDBN Hereditary cutaneous melanoma
Reversed 1
HGVS NC_000009.11:g.21974685G>T
CLNSRC
CLNACC RCV000168272.1,