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rs786203329

From SNPedia

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


Make rs786203329(-;-)
ReferenceGRCh38.p2 38.2/146
Chromosome13
Position32337708
GeneBRCA2
is asnp
is mentioned by
dbSNPrs786203329
dbSNP (old)rs786203329
ClinGenrs786203329
ebirs786203329
HLIrs786203329
Exacrs786203329
Varsomers786203329
Maprs786203329
PheGenIrs786203329
Biobankrs786203329
1000 genomesrs786203329
hgdprs786203329
ensemblrs786203329
gopubmedrs786203329
geneviewrs786203329
scholarrs786203329
googlers786203329
pharmgkbrs786203329
gwascentralrs786203329
openSNPrs786203329
23andMers786203329
23andMe allrs786203329
SNP Nexus

SNPshotrs786203329
SNPdbers786203329
MSV3drs786203329
GWAS Ctlgrs786203329
Max Magnitude6
ClinVar
Risk rs786203329(-;-)
Alt rs786203329(-;-)
Reference Rs786203329(TAG;TAG)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome Breast-ovarian cancer not provided
Variation info
Gene BRCA2
CLNDBN Hereditary cancer-predisposing syndrome Breast-ovarian cancer, familial 2 not provided
Reversed 0
HGVS NC_000013.10:g.32911845_32911847delTAG
CLNSRC
CLNACC RCV000166594.1, RCV000241307.2, RCV000481570.1,