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rs876660311

From SNPedia

Orientationplus
Geno Mag Summary
(ATGGC;ATGGC) 0 common in clinvar
Make rs876660311(-;-)
Make rs876660311(-;TGGCA)
Make rs876660311(TGGCA;TGGCA)
ReferenceGRCh38.p2 38.2/147
Chromosome13
Position32340024
GeneBRCA2
is asnp
is mentioned by
dbSNPrs876660311
ebirs876660311
HLIrs876660311
Exacrs876660311
Varsomers876660311
Maprs876660311
PheGenIrs876660311
hapmaprs876660311
1000 genomesrs876660311
hgdprs876660311
ensemblrs876660311
gopubmedrs876660311
geneviewrs876660311
scholarrs876660311
googlers876660311
pharmgkbrs876660311
gwascentralrs876660311
openSNPrs876660311
23andMers876660311
23andMe allrs876660311
SNP Nexus

SNPshotrs876660311
SNPdbers876660311
MSV3drs876660311
GWAS Ctlgrs876660311
Max Magnitude0
ClinVar
Risk rs876660311(;)
Alt rs876660311(;)
Reference rs876660311(ATGGC;ATGGC)
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.32914161_32914165delTGGCA
CLNSRC
CLNACC RCV000217920.1,