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rs876659317

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs876659317(-;-)
Make rs876659317(-;GT)
Make rs876659317(GT;GT)
ReferenceGRCh38.p2 38.2/147
Chromosome13
Position32326127
GeneBRCA2
is asnp
is mentioned by
dbSNPrs876659317
ebirs876659317
HLIrs876659317
Exacrs876659317
Varsomers876659317
Maprs876659317
PheGenIrs876659317
hapmaprs876659317
1000 genomesrs876659317
hgdprs876659317
ensemblrs876659317
gopubmedrs876659317
geneviewrs876659317
scholarrs876659317
googlers876659317
pharmgkbrs876659317
gwascentralrs876659317
openSNPrs876659317
23andMers876659317
23andMe allrs876659317
SNP Nexus

SNPshotrs876659317
SNPdbers876659317
MSV3drs876659317
GWAS Ctlgrs876659317
Max Magnitude0
ClinVar
Risk rs876659317(TG;TG)
Alt rs876659317(TG;TG)
Reference rs876659317(;)
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.32900263_32900264dupGT
CLNSRC
CLNACC RCV000219448.1,