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

rs36204594

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs36204594(C;T)
Make rs36204594(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome9
Position21971180
GeneCDKN2A
is asnp
is mentioned by
dbSNPrs36204594
ebirs36204594
HLIrs36204594
Exacrs36204594
Varsomers36204594
Maprs36204594
PheGenIrs36204594
hapmaprs36204594
1000 genomesrs36204594
hgdprs36204594
ensemblrs36204594
gopubmedrs36204594
geneviewrs36204594
scholarrs36204594
googlers36204594
pharmgkbrs36204594
gwascentralrs36204594
openSNPrs36204594
23andMers36204594
23andMe allrs36204594
SNP Nexus

SNPshotrs36204594
SNPdbers36204594
MSV3drs36204594
GWAS Ctlgrs36204594
Max Magnitude0
ClinVar
Risk rs36204594(A;A)
Alt rs36204594(A;A)
Reference rs36204594(C;C)
Significance Probable-Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene CDKN2A
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 1
HGVS NC_000009.11:g.21971179G>T
CLNSRC
CLNACC RCV000165798.1,