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rs786203853

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(-;-) 0 common in clinvar
(-;T) 6 BRCA2 variant considered pathogenic for breast cancer
Make rs786203853(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome13
Position32339851
GeneBRCA2
is asnp
is mentioned by
dbSNPrs786203853
dbSNP (old)rs786203853
ClinGenrs786203853
ebirs786203853
HLIrs786203853
Exacrs786203853
Gnomadrs786203853
Varsomers786203853
Maprs786203853
PheGenIrs786203853
Biobankrs786203853
1000 genomesrs786203853
hgdprs786203853
ensemblrs786203853
gopubmedrs786203853
geneviewrs786203853
scholarrs786203853
googlers786203853
pharmgkbrs786203853
gwascentralrs786203853
openSNPrs786203853
23andMers786203853
23andMe allrs786203853
SNP Nexus

SNPshotrs786203853
SNPdbers786203853
MSV3drs786203853
GWAS Ctlgrs786203853
Max Magnitude6
ClinVar
Risk rs786203853(T;T)
Alt rs786203853(T;T)
Reference Rs786203853(-;-)
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.32913988dupT
CLNSRC
CLNACC RCV000167340.1, RCV000241246.1,