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rs786203587

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
(G;T) 6 BRCA1 variant considered pathogenic for breast cancer
Make rs786203587(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome17
Position43092374
GeneBRCA1
is asnp
is mentioned by
dbSNPrs786203587
dbSNP (old)rs786203587
ClinGenrs786203587
ebirs786203587
HLIrs786203587
Exacrs786203587
Gnomadrs786203587
Varsomers786203587
Maprs786203587
PheGenIrs786203587
Biobankrs786203587
1000 genomesrs786203587
hgdprs786203587
ensemblrs786203587
gopubmedrs786203587
geneviewrs786203587
scholarrs786203587
googlers786203587
pharmgkbrs786203587
gwascentralrs786203587
openSNPrs786203587
23andMers786203587
23andMe allrs786203587
SNP Nexus

SNPshotrs786203587
SNPdbers786203587
MSV3drs786203587
GWAS Ctlgrs786203587
Max Magnitude6
ClinVar
Risk rs786203587(T;T)
Alt rs786203587(T;T)
Reference Rs786203587(G;G)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome Breast-ovarian cancer
Variation info
Gene BRCA1
CLNDBN Hereditary cancer-predisposing syndrome Breast-ovarian cancer, familial 1
Reversed 1
HGVS NC_000017.10:g.41244391C>A
CLNSRC
CLNACC RCV000166966.2, RCV000241281.1,