Have questions? Visit https://www.reddit.com/r/SNPedia

rs786202385

From SNPedia

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


Make rs786202385(-;-)
ReferenceGRCh38.p2 38.2/146
Chromosome13
Position32339708
GeneBRCA2
is asnp
is mentioned by
dbSNPrs786202385
dbSNP (old)rs786202385
ClinGenrs786202385
ebirs786202385
HLIrs786202385
Exacrs786202385
Varsomers786202385
Maprs786202385
PheGenIrs786202385
Biobankrs786202385
1000 genomesrs786202385
hgdprs786202385
ensemblrs786202385
gopubmedrs786202385
geneviewrs786202385
scholarrs786202385
googlers786202385
pharmgkbrs786202385
gwascentralrs786202385
openSNPrs786202385
23andMers786202385
23andMe allrs786202385
SNP Nexus

SNPshotrs786202385
SNPdbers786202385
MSV3drs786202385
GWAS Ctlgrs786202385
Max Magnitude6
ClinVar
Risk rs786202385(-;-)
Alt rs786202385(-;-)
Reference Rs786202385(A;A)
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.32913845delA
CLNSRC
CLNACC RCV000165166.1, RCV000241267.2,