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rs786202061

From SNPedia

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


Make rs786202061(-;-)
ReferenceGRCh38.p2 38.2/146
Chromosome13
Position32340118
GeneBRCA2
is asnp
is mentioned by
dbSNPrs786202061
dbSNP (old)rs786202061
ClinGenrs786202061
ebirs786202061
HLIrs786202061
Exacrs786202061
Varsomers786202061
Maprs786202061
PheGenIrs786202061
Biobankrs786202061
1000 genomesrs786202061
hgdprs786202061
ensemblrs786202061
gopubmedrs786202061
geneviewrs786202061
scholarrs786202061
googlers786202061
pharmgkbrs786202061
gwascentralrs786202061
openSNPrs786202061
23andMers786202061
23andMe allrs786202061
SNP Nexus

SNPshotrs786202061
SNPdbers786202061
MSV3drs786202061
GWAS Ctlgrs786202061
Max Magnitude6
ClinVar
Risk rs786202061(-;-)
Alt rs786202061(-;-)
Reference Rs786202061(T;T)
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.32914255delT
CLNSRC
CLNACC RCV000164683.1, RCV000241035.1,