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rs587778189

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs587778189(A;T)
Make rs587778189(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome9
Position21974679
GeneCDKN2A
is asnp
is mentioned by
dbSNPrs587778189
ebirs587778189
HLIrs587778189
Exacrs587778189
Varsomers587778189
Maprs587778189
PheGenIrs587778189
hapmaprs587778189
1000 genomesrs587778189
hgdprs587778189
ensemblrs587778189
gopubmedrs587778189
geneviewrs587778189
scholarrs587778189
googlers587778189
pharmgkbrs587778189
gwascentralrs587778189
openSNPrs587778189
23andMers587778189
23andMe allrs587778189
SNP Nexus

SNPshotrs587778189
SNPdbers587778189
MSV3drs587778189
GWAS Ctlgrs587778189
Max Magnitude0
ClinVar
Risk rs587778189(C,G,T;C,G,T)
Alt rs587778189(C,G,T;C,G,T)
Reference rs587778189(A;A)
Significance Probable-Pathogenic
Disease not specified Tumor susceptibility linked to germline BAP1 mutations Hereditary cancer-predisposing syndrome
Variation info
Gene CDKN2A
CLNDBN not specified Tumor susceptibility linked to germline BAP1 mutations Hereditary cancer-predisposing syndrome
Reversed 1
HGVS NC_000009.11:g.21974678T>A; NC_000009.11:g.21974678T>C; NC_000009.11:g.21974678T>G
CLNSRC
CLNACC RCV000120538.1, RCV000213788.1, RCV000167463.1,