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rs786203432

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(-;-) 0 common in clinvar
(-;A) 6 BRCA1 variant considered pathogenic for breast cancer
Make rs786203432(A;A)
ReferenceGRCh38.p2 38.2/146
Chromosome17
Position43104146
GeneBRCA1
is asnp
is mentioned by
dbSNPrs786203432
dbSNP (old)rs786203432
ClinGenrs786203432
ebirs786203432
HLIrs786203432
Exacrs786203432
Gnomadrs786203432
Varsomers786203432
Maprs786203432
PheGenIrs786203432
Biobankrs786203432
1000 genomesrs786203432
hgdprs786203432
ensemblrs786203432
gopubmedrs786203432
geneviewrs786203432
scholarrs786203432
googlers786203432
pharmgkbrs786203432
gwascentralrs786203432
openSNPrs786203432
23andMers786203432
23andMe allrs786203432
SNP Nexus

SNPshotrs786203432
SNPdbers786203432
MSV3drs786203432
GWAS Ctlgrs786203432
Max Magnitude6
ClinVar
Risk rs786203432(A;A)
Alt rs786203432(A;A)
Reference Rs786203432(-;-)
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.41256164dupT
CLNSRC
CLNACC RCV000166734.1, RCV000241128.2,