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rs786203592

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(-;-) 0 common in clinvar
(-;T) 6 BRCA1 variant considered pathogenic for breast cancer
Make rs786203592(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome17
Position43092876
GeneBRCA1
is asnp
is mentioned by
dbSNPrs786203592
dbSNP (old)rs786203592
ClinGenrs786203592
ebirs786203592
HLIrs786203592
Exacrs786203592
Gnomadrs786203592
Varsomers786203592
Maprs786203592
PheGenIrs786203592
Biobankrs786203592
1000 genomesrs786203592
hgdprs786203592
ensemblrs786203592
gopubmedrs786203592
geneviewrs786203592
scholarrs786203592
googlers786203592
pharmgkbrs786203592
gwascentralrs786203592
openSNPrs786203592
23andMers786203592
23andMe allrs786203592
SNP Nexus

SNPshotrs786203592
SNPdbers786203592
MSV3drs786203592
GWAS Ctlgrs786203592
Max Magnitude6
ClinVar
Risk rs786203592(T;T)
Alt rs786203592(T;T)
Reference Rs786203592(-;-)
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.41244894dupA
CLNSRC
CLNACC RCV000166972.1, RCV000241185.1,