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rs786201986

From SNPedia

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


Make rs786201986(-;-)
ReferenceGRCh38.p2 38.2/146
Chromosome13
Position32333030
GeneBRCA2
is asnp
is mentioned by
dbSNPrs786201986
ClinGenrs786201986
ebirs786201986
HLIrs786201986
Exacrs786201986
Varsomers786201986
Maprs786201986
PheGenIrs786201986
hapmaprs786201986
1000 genomesrs786201986
hgdprs786201986
ensemblrs786201986
gopubmedrs786201986
geneviewrs786201986
scholarrs786201986
googlers786201986
pharmgkbrs786201986
gwascentralrs786201986
openSNPrs786201986
23andMers786201986
23andMe allrs786201986
SNP Nexus

SNPshotrs786201986
SNPdbers786201986
MSV3drs786201986
GWAS Ctlgrs786201986
Max Magnitude6
ClinVar
Risk rs786201986(-;-)
Alt rs786201986(-;-)
Reference Rs786201986(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.32907167delG
CLNSRC
CLNACC RCV000164549.1, RCV000241159.1,