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

rs876660637

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs876660637(-;-)
Make rs876660637(-;A)
ReferenceGRCh38.p2 38.2/147
Chromosome13
Position32340394
GeneBRCA2
is asnp
is mentioned by
dbSNPrs876660637
ebirs876660637
HLIrs876660637
Exacrs876660637
Varsomers876660637
Maprs876660637
PheGenIrs876660637
hapmaprs876660637
1000 genomesrs876660637
hgdprs876660637
ensemblrs876660637
gopubmedrs876660637
geneviewrs876660637
scholarrs876660637
googlers876660637
pharmgkbrs876660637
gwascentralrs876660637
openSNPrs876660637
23andMers876660637
23andMe allrs876660637
SNP Nexus

SNPshotrs876660637
SNPdbers876660637
MSV3drs876660637
GWAS Ctlgrs876660637
Max Magnitude0
ClinVar
Risk rs876660637(;)
Alt rs876660637(;)
Reference rs876660637(A;A)
Significance Pathogenic
Disease Tumor susceptibility linked to germline BAP1 mutations
Variation info
Gene BRCA2
CLNDBN Tumor susceptibility linked to germline BAP1 mutations
Reversed 0
HGVS NC_000013.10:g.32914531delA
CLNSRC
CLNACC RCV000216951.1,