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rs786203103

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(-;-) 0 common in clinvar
(-;T) 6 BRCA1 variant considered pathogenic for breast cancer
Make rs786203103(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome17
Position43094274
GeneBRCA1
is asnp
is mentioned by
dbSNPrs786203103
dbSNP (old)rs786203103
ClinGenrs786203103
ebirs786203103
HLIrs786203103
Exacrs786203103
Gnomadrs786203103
Varsomers786203103
Maprs786203103
PheGenIrs786203103
Biobankrs786203103
1000 genomesrs786203103
hgdprs786203103
ensemblrs786203103
gopubmedrs786203103
geneviewrs786203103
scholarrs786203103
googlers786203103
pharmgkbrs786203103
gwascentralrs786203103
openSNPrs786203103
23andMers786203103
23andMe allrs786203103
SNP Nexus

SNPshotrs786203103
SNPdbers786203103
MSV3drs786203103
GWAS Ctlgrs786203103
Max Magnitude6
ClinVar
Risk rs786203103(T;T)
Alt rs786203103(T;T)
Reference Rs786203103(-;-)
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.41246292dupA
CLNSRC
CLNACC RCV000166261.1, RCV000240975.1,