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

rs876659862

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs876659862(-;-)
Make rs876659862(-;T)
ReferenceGRCh38.p2 38.2/147
Chromosome13
Position32336856
GeneBRCA2
is asnp
is mentioned by
dbSNPrs876659862
ebirs876659862
HLIrs876659862
Exacrs876659862
Varsomers876659862
Maprs876659862
PheGenIrs876659862
hapmaprs876659862
1000 genomesrs876659862
hgdprs876659862
ensemblrs876659862
gopubmedrs876659862
geneviewrs876659862
scholarrs876659862
googlers876659862
pharmgkbrs876659862
gwascentralrs876659862
openSNPrs876659862
23andMers876659862
23andMe allrs876659862
SNP Nexus

SNPshotrs876659862
SNPdbers876659862
MSV3drs876659862
GWAS Ctlgrs876659862
Max Magnitude0
ClinVar
Risk rs876659862(;)
Alt rs876659862(;)
Reference rs876659862(T;T)
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.32910993delT
CLNSRC
CLNACC RCV000218765.1,