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

rs876660541

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs876660541(-;-)
Make rs876660541(-;TTTT)
Make rs876660541(TTTT;TTTT)
ReferenceGRCh38.p2 38.2/147
Chromosome13
Position32341057
GeneBRCA2
is asnp
is mentioned by
dbSNPrs876660541
ebirs876660541
HLIrs876660541
Exacrs876660541
Varsomers876660541
Maprs876660541
PheGenIrs876660541
hapmaprs876660541
1000 genomesrs876660541
hgdprs876660541
ensemblrs876660541
gopubmedrs876660541
geneviewrs876660541
scholarrs876660541
googlers876660541
pharmgkbrs876660541
gwascentralrs876660541
openSNPrs876660541
23andMers876660541
23andMe allrs876660541
SNP Nexus

SNPshotrs876660541
SNPdbers876660541
MSV3drs876660541
GWAS Ctlgrs876660541
Max Magnitude0
ClinVar
Risk rs876660541(TTTT;TTTT)
Alt rs876660541(TTTT;TTTT)
Reference rs876660541(;)
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.32915191_32915194dupTTTT
CLNSRC
CLNACC RCV000215061.1,