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rs876658556

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs876658556(A;A)
Make rs876658556(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome9
Position21974784
GeneCDKN2A
is asnp
is mentioned by
dbSNPrs876658556
ebirs876658556
HLIrs876658556
Exacrs876658556
Varsomers876658556
Maprs876658556
PheGenIrs876658556
hapmaprs876658556
1000 genomesrs876658556
hgdprs876658556
ensemblrs876658556
gopubmedrs876658556
geneviewrs876658556
scholarrs876658556
googlers876658556
pharmgkbrs876658556
gwascentralrs876658556
openSNPrs876658556
23andMers876658556
23andMe allrs876658556
SNP Nexus

SNPshotrs876658556
SNPdbers876658556
MSV3drs876658556
GWAS Ctlgrs876658556
Max Magnitude0
ClinVar
Risk rs876658556(A;A)
Alt rs876658556(A;A)
Reference rs876658556(G;G)
Significance 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.21974783C>T
CLNSRC
CLNACC RCV000220239.1,