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rs767234936

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(-;G) 6 BRCA2 variant considered pathogenic for breast cancer
(G;G) 0 common in clinvar


Make rs767234936(-;-)
ReferenceGRCh38.p2 38.2/147
Chromosome13
Position32338600
GeneBRCA2
is asnp
is mentioned by
dbSNPrs767234936
dbSNP (old)rs767234936
ClinGenrs767234936
ebirs767234936
HLIrs767234936
Exacrs767234936
Gnomadrs767234936
Varsomers767234936
Maprs767234936
PheGenIrs767234936
Biobankrs767234936
1000 genomesrs767234936
hgdprs767234936
ensemblrs767234936
gopubmedrs767234936
geneviewrs767234936
scholarrs767234936
googlers767234936
pharmgkbrs767234936
gwascentralrs767234936
openSNPrs767234936
23andMers767234936
23andMe allrs767234936
SNP Nexus

SNPshotrs767234936
SNPdbers767234936
MSV3drs767234936
GWAS Ctlgrs767234936
Max Magnitude6
ClinVar
Risk rs767234936(-;-)
Alt rs767234936(-;-)
Reference Rs767234936(G;G)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome Breast-ovarian cancer
Variation info
Gene BRCA2
CLNDBN Hereditary cancer-predisposing syndrome Breast-ovarian cancer, familial 2
Reversed 0
HGVS NC_000013.10:g.32912737delG
CLNSRC
CLNACC RCV000219417.1, RCV000241053.1,