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

rs876658654

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs876658654(-;-)
Make rs876658654(-;C)
ReferenceGRCh38.p2 38.2/147
Chromosome13
Position32338988
GeneBRCA2
is asnp
is mentioned by
dbSNPrs876658654
ebirs876658654
HLIrs876658654
Exacrs876658654
Varsomers876658654
Maprs876658654
PheGenIrs876658654
hapmaprs876658654
1000 genomesrs876658654
hgdprs876658654
ensemblrs876658654
gopubmedrs876658654
geneviewrs876658654
scholarrs876658654
googlers876658654
pharmgkbrs876658654
gwascentralrs876658654
openSNPrs876658654
23andMers876658654
23andMe allrs876658654
SNP Nexus

SNPshotrs876658654
SNPdbers876658654
MSV3drs876658654
GWAS Ctlgrs876658654
Max Magnitude0
ClinVar
Risk rs876658654(;)
Alt rs876658654(;)
Reference rs876658654(C;C)
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.32913125delC
CLNSRC
CLNACC RCV000218310.1,