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

rs786202441

From SNPedia

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


Make rs786202441(-;-)
ReferenceGRCh38.p2 38.2/146
Chromosome13
Position32355154
GeneBRCA2
is asnp
is mentioned by
dbSNPrs786202441
ClinGenrs786202441
ebirs786202441
HLIrs786202441
Exacrs786202441
Varsomers786202441
Maprs786202441
PheGenIrs786202441
hapmaprs786202441
1000 genomesrs786202441
hgdprs786202441
ensemblrs786202441
gopubmedrs786202441
geneviewrs786202441
scholarrs786202441
googlers786202441
pharmgkbrs786202441
gwascentralrs786202441
openSNPrs786202441
23andMers786202441
23andMe allrs786202441
SNP Nexus

SNPshotrs786202441
SNPdbers786202441
MSV3drs786202441
GWAS Ctlgrs786202441
Max Magnitude6
ClinVar
Risk rs786202441(-;-)
Alt rs786202441(-;-)
Reference Rs786202441(A;A)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome Breast-ovarian cancer Hereditary breast and ovarian cancer syndrome
Variation info
Gene BRCA2
CLNDBN Hereditary cancer-predisposing syndrome Breast-ovarian cancer, familial 2 Hereditary breast and ovarian cancer syndrome
Reversed 0
HGVS NC_000013.10:g.32929291delA
CLNSRC
CLNACC RCV000165253.1, RCV000238842.3, RCV000474906.1,