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rs786203660

From SNPedia

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


Make rs786203660(-;-)
ReferenceGRCh38.p2 38.2/146
Chromosome13
Position32340813
GeneBRCA2
is asnp
is mentioned by
dbSNPrs786203660
dbSNP (old)rs786203660
ClinGenrs786203660
ebirs786203660
HLIrs786203660
Exacrs786203660
Varsomers786203660
Maprs786203660
PheGenIrs786203660
Biobankrs786203660
1000 genomesrs786203660
hgdprs786203660
ensemblrs786203660
gopubmedrs786203660
geneviewrs786203660
scholarrs786203660
googlers786203660
pharmgkbrs786203660
gwascentralrs786203660
openSNPrs786203660
23andMers786203660
23andMe allrs786203660
SNP Nexus

SNPshotrs786203660
SNPdbers786203660
MSV3drs786203660
GWAS Ctlgrs786203660
Max Magnitude6
ClinVar
Risk rs786203660(-;-)
Alt rs786203660(-;-)
Reference Rs786203660(C;C)
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.32914950delC
CLNSRC
CLNACC RCV000167067.1, RCV000238738.2,