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rs431825385

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(-;-) 0 common in clinvar
(-;T) 6 BRCA1 variant considered pathogenic for breast cancer
Make rs431825385(T;T)
ReferenceGRCh38 38.1/141
Chromosome17
Position43115729
GeneBRCA1
is asnp
is mentioned by
dbSNPrs431825385
dbSNP (classic)rs431825385
ClinGenrs431825385
ebirs431825385
HLIrs431825385
Exacrs431825385
Gnomadrs431825385
Varsomers431825385
LitVarrs431825385
Maprs431825385
PheGenIrs431825385
Biobankrs431825385
1000 genomesrs431825385
hgdprs431825385
ensemblrs431825385
geneviewrs431825385
scholarrs431825385
googlers431825385
pharmgkbrs431825385
gwascentralrs431825385
openSNPrs431825385
23andMers431825385
SNPshotrs431825385
SNPdbers431825385
MSV3drs431825385
GWAS Ctlgrs431825385
Max Magnitude6

rs431825385 has merged into rs80357951

ClinVar
Risk rs431825385(T;T)
Alt rs431825385(T;T)
Reference Rs431825385(-;-)
Significance Pathogenic
Disease Breast-ovarian cancer
Variation info
Gene BRCA1
CLNDBN Breast-ovarian cancer, familial 1
Reversed 1
HGVS NC_000017.10:g.41267747dupA
CLNSRC ClinVar
CLNACC RCV000083019.3,