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rs121913388

From SNPedia

Orientationminus
Stabilizedminus
Make rs121913388(C;C)
Make rs121913388(C;T)
Make rs121913388(T;T)
ReferenceGRCh38 38.1/141
Chromosome9
Position21971121
GeneCDKN2A
is asnp
is mentioned by
dbSNPrs121913388
dbSNP (old)rs121913388
ClinGenrs121913388
ebirs121913388
HLIrs121913388
Exacrs121913388
Gnomadrs121913388
Varsomers121913388
Maprs121913388
PheGenIrs121913388
Biobankrs121913388
1000 genomesrs121913388
hgdprs121913388
ensemblrs121913388
gopubmedrs121913388
geneviewrs121913388
scholarrs121913388
googlers121913388
pharmgkbrs121913388
gwascentralrs121913388
openSNPrs121913388
23andMers121913388
23andMe allrs121913388
SNP Nexus

SNPshotrs121913388
SNPdbers121913388
MSV3drs121913388
GWAS Ctlgrs121913388
Max Magnitude
OMIM600160
Desc
Variant0002
Relatedalso
ClinVar
Risk rs121913388(G;G) rs121913388(T;T)
Alt rs121913388(G;G) rs121913388(T;T)
Reference rs121913388(C;C)
Significance Other
Disease Melanoma Malignant melanoma
Variation info
Gene CDKN2A
CLNDBN Melanoma, cutaneous malignant, susceptibility to, 2 Malignant melanoma
Reversed 1
HGVS NC_000009.11:g.21971120G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000010012.2, RCV000429694.1,


[PMID 21499247OA-icon.png] Exome sequencing identifies GRIN2A as frequently mutated in melanoma.