Have questions? Visit https://www.reddit.com/r/SNPedia

rs372670098

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs372670098(C;C)
Make rs372670098(C;T)
ReferenceGRCh38.p2 38.2/144
Chromosome9
Position21971153
GeneCDKN2A
is asnp
is mentioned by
dbSNPrs372670098
ebirs372670098
HLIrs372670098
Exacrs372670098
Varsomers372670098
Maprs372670098
PheGenIrs372670098
hapmaprs372670098
1000 genomesrs372670098
hgdprs372670098
ensemblrs372670098
gopubmedrs372670098
geneviewrs372670098
scholarrs372670098
googlers372670098
pharmgkbrs372670098
gwascentralrs372670098
openSNPrs372670098
23andMers372670098
23andMe allrs372670098
SNP Nexus

SNPshotrs372670098
SNPdbers372670098
MSV3drs372670098
GWAS Ctlgrs372670098
Max Magnitude0
ClinVar
Risk rs372670098(C;C)
Alt rs372670098(C;C)
Reference rs372670098(T;T)
Significance Probable-Pathogenic
Disease Hereditary cancer-predisposing syndrome Hereditary cutaneous melanoma not specified
Variation info
Gene CDKN2A
CLNDBN Hereditary cancer-predisposing syndrome Hereditary cutaneous melanoma not specified
Reversed 0
HGVS NC_000009.11:g.21971152T>C
CLNSRC
CLNACC RCV000166237.1, RCV000205699.1, RCV000235616.1,