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rs786203594

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(-;A) 6 BRCA1 variant considered pathogenic for breast cancer
(A;A) 0 common in clinvar


Make rs786203594(-;-)
ReferenceGRCh38.p2 38.2/146
Chromosome17
Position43093567
GeneBRCA1
is asnp
is mentioned by
dbSNPrs786203594
dbSNP (old)rs786203594
ClinGenrs786203594
ebirs786203594
HLIrs786203594
Exacrs786203594
Gnomadrs786203594
Varsomers786203594
Maprs786203594
PheGenIrs786203594
Biobankrs786203594
1000 genomesrs786203594
hgdprs786203594
ensemblrs786203594
gopubmedrs786203594
geneviewrs786203594
scholarrs786203594
googlers786203594
pharmgkbrs786203594
gwascentralrs786203594
openSNPrs786203594
23andMers786203594
23andMe allrs786203594
SNP Nexus

SNPshotrs786203594
SNPdbers786203594
MSV3drs786203594
GWAS Ctlgrs786203594
Max Magnitude6
ClinVar
Risk rs786203594(-;-)
Alt rs786203594(-;-)
Reference Rs786203594(A;A)
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.41245584delT
CLNSRC
CLNACC RCV000166975.1, RCV000241082.1,