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rs876658534

From SNPedia

Orientationminus
Geno Mag Summary
(GC;GC) 0 common in clinvar
Make rs876658534(GC;TT)
Make rs876658534(TT;TT)
ReferenceGRCh38.p2 38.2/147
Chromosome9
Position21971156
GeneCDKN2A
is asnp
is mentioned by
dbSNPrs876658534
ebirs876658534
HLIrs876658534
Exacrs876658534
Varsomers876658534
Maprs876658534
PheGenIrs876658534
hapmaprs876658534
1000 genomesrs876658534
hgdprs876658534
ensemblrs876658534
gopubmedrs876658534
geneviewrs876658534
scholarrs876658534
googlers876658534
pharmgkbrs876658534
gwascentralrs876658534
openSNPrs876658534
23andMers876658534
23andMe allrs876658534
SNP Nexus

SNPshotrs876658534
SNPdbers876658534
MSV3drs876658534
GWAS Ctlgrs876658534
Max Magnitude0
ClinVar
Risk rs876658534(TT;TT)
Alt rs876658534(TT;TT)
Reference rs876658534(GC;GC)
Significance Probable-Pathogenic
Disease Tumor susceptibility linked to germline BAP1 mutations
Variation info
Gene CDKN2A
CLNDBN Tumor susceptibility linked to germline BAP1 mutations
Reversed 1
HGVS NC_000009.11:g.21971155_21971156delGCinsAA
CLNSRC
CLNACC RCV000213270.1,