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rs431825414

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(;) 0 common in clinvar
(-;C) 6 BRCA1 variant considered pathogenic for breast cancer
Make rs431825414(-;-)
Make rs431825414(C;C)
ReferenceGRCh38 38.1/141
Chromosome17
Position43057060
GeneBRCA1
is asnp
is mentioned by
dbSNPrs431825414
ClinGenrs431825414
ebirs431825414
HLIrs431825414
Exacrs431825414
Varsomers431825414
Maprs431825414
PheGenIrs431825414
hapmaprs431825414
1000 genomesrs431825414
hgdprs431825414
ensemblrs431825414
gopubmedrs431825414
geneviewrs431825414
scholarrs431825414
googlers431825414
pharmgkbrs431825414
gwascentralrs431825414
openSNPrs431825414
23andMers431825414
23andMe allrs431825414
SNP Nexus

SNPshotrs431825414
SNPdbers431825414
MSV3drs431825414
GWAS Ctlgrs431825414
Max Magnitude6
ClinVar
Risk rs431825414(C;C)
Alt rs431825414(C;C)
Reference Rs431825414(;)
Significance Pathogenic
Disease Breast-ovarian cancer
Variation info
Gene BRCA1
CLNDBN Breast-ovarian cancer, familial 1
Reversed 1
HGVS NC_000017.10:g.41209077_41209078insG
CLNSRC ClinVar
CLNACC RCV000083067.2,