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rs786203546

From SNPedia

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


Make rs786203546(-;-)
ReferenceGRCh38.p2 38.2/146
Chromosome13
Position32354879
GeneBRCA2
is asnp
is mentioned by
dbSNPrs786203546
dbSNP (old)rs786203546
ClinGenrs786203546
ebirs786203546
HLIrs786203546
Exacrs786203546
Gnomadrs786203546
Varsomers786203546
Maprs786203546
PheGenIrs786203546
Biobankrs786203546
1000 genomesrs786203546
hgdprs786203546
ensemblrs786203546
gopubmedrs786203546
geneviewrs786203546
scholarrs786203546
googlers786203546
pharmgkbrs786203546
gwascentralrs786203546
openSNPrs786203546
23andMers786203546
23andMe allrs786203546
SNP Nexus

SNPshotrs786203546
SNPdbers786203546
MSV3drs786203546
GWAS Ctlgrs786203546
Max Magnitude6
ClinVar
Risk rs786203546(-;-)
Alt rs786203546(-;-)
Reference Rs786203546(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.32929016delA
CLNSRC
CLNACC RCV000166905.1, RCV000241486.1,