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rs876660421

From SNPedia

Orientationplus
Geno Mag Summary
(TT;TT) 0 common in clinvar
Make rs876660421(-;-)
Make rs876660421(-;TT)
ReferenceGRCh38.p2 38.2/147
Chromosome13
Position32340801
GeneBRCA2
is asnp
is mentioned by
dbSNPrs876660421
ebirs876660421
HLIrs876660421
Exacrs876660421
Varsomers876660421
Maprs876660421
PheGenIrs876660421
hapmaprs876660421
1000 genomesrs876660421
hgdprs876660421
ensemblrs876660421
gopubmedrs876660421
geneviewrs876660421
scholarrs876660421
googlers876660421
pharmgkbrs876660421
gwascentralrs876660421
openSNPrs876660421
23andMers876660421
23andMe allrs876660421
SNP Nexus

SNPshotrs876660421
SNPdbers876660421
MSV3drs876660421
GWAS Ctlgrs876660421
Max Magnitude0
ClinVar
Risk rs876660421(;)
Alt rs876660421(;)
Reference rs876660421(TT;TT)
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.32914938_32914939delTT
CLNSRC
CLNACC RCV000222779.1,