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rs786203575

From SNPedia

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


Make rs786203575(-;-)
ReferenceGRCh38.p2 38.2/146
Chromosome13
Position32379821
GeneBRCA2
is asnp
is mentioned by
dbSNPrs786203575
ClinGenrs786203575
ebirs786203575
HLIrs786203575
Exacrs786203575
Varsomers786203575
Maprs786203575
PheGenIrs786203575
hapmaprs786203575
1000 genomesrs786203575
hgdprs786203575
ensemblrs786203575
gopubmedrs786203575
geneviewrs786203575
scholarrs786203575
googlers786203575
pharmgkbrs786203575
gwascentralrs786203575
openSNPrs786203575
23andMers786203575
23andMe allrs786203575
SNP Nexus

SNPshotrs786203575
SNPdbers786203575
MSV3drs786203575
GWAS Ctlgrs786203575
Max Magnitude6
ClinVar
Risk rs786203575(-;-)
Alt rs786203575(-;-)
Reference Rs786203575(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.32953958delT
CLNSRC
CLNACC RCV000166953.1, RCV000241186.2,