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rs786203537

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(-;-) 0 common in clinvar
(-;A) 6 BRCA2 variant considered pathogenic for breast cancer
Make rs786203537(A;A)
ReferenceGRCh38.p2 38.2/146
Chromosome13
Position32338191
GeneBRCA2
is asnp
is mentioned by
dbSNPrs786203537
ClinGenrs786203537
ebirs786203537
HLIrs786203537
Exacrs786203537
Varsomers786203537
Maprs786203537
PheGenIrs786203537
hapmaprs786203537
1000 genomesrs786203537
hgdprs786203537
ensemblrs786203537
gopubmedrs786203537
geneviewrs786203537
scholarrs786203537
googlers786203537
pharmgkbrs786203537
gwascentralrs786203537
openSNPrs786203537
23andMers786203537
23andMe allrs786203537
SNP Nexus

SNPshotrs786203537
SNPdbers786203537
MSV3drs786203537
GWAS Ctlgrs786203537
Max Magnitude6
ClinVar
Risk rs786203537(A;A)
Alt rs786203537(A;A)
Reference Rs786203537(-;-)
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.32912328dupA
CLNSRC
CLNACC RCV000166888.1, RCV000241488.1,