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rs767234936

From SNPedia

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Geno Mag Summary
(G;G) 0 common in clinvar
Make rs767234936(-;-)
Make rs767234936(-;G)
ReferenceGRCh38.p2 38.2/147
Chromosome13
Position32338600
GeneBRCA2
is asnp
is mentioned by
dbSNPrs767234936
ebirs767234936
HLIrs767234936
Exacrs767234936
Varsomers767234936
Maprs767234936
PheGenIrs767234936
hapmaprs767234936
1000 genomesrs767234936
hgdprs767234936
ensemblrs767234936
gopubmedrs767234936
geneviewrs767234936
scholarrs767234936
googlers767234936
pharmgkbrs767234936
gwascentralrs767234936
openSNPrs767234936
23andMers767234936
23andMe allrs767234936
SNP Nexus

SNPshotrs767234936
SNPdbers767234936
MSV3drs767234936
GWAS Ctlgrs767234936
Max Magnitude0
ClinVar
Risk rs767234936(;)
Alt rs767234936(;)
Reference rs767234936(G;G)
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.32912737delG
CLNSRC
CLNACC RCV000219417.1,