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rs431825413

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs431825413(-;-)
Make rs431825413(-;C)
Make rs431825413(C;C)
ReferenceGRCh38 38.1/141
Chromosome17
Position43057064
GeneBRCA1
is asnp
is mentioned by
dbSNPrs431825413
ebirs431825413
HLIrs431825413
Exacrs431825413
Varsomers431825413
Maprs431825413
PheGenIrs431825413
hapmaprs431825413
1000 genomesrs431825413
hgdprs431825413
ensemblrs431825413
gopubmedrs431825413
geneviewrs431825413
scholarrs431825413
googlers431825413
pharmgkbrs431825413
gwascentralrs431825413
openSNPrs431825413
23andMers431825413
23andMe allrs431825413
SNP Nexus

SNPshotrs431825413
SNPdbers431825413
MSV3drs431825413
GWAS Ctlgrs431825413
Max Magnitude0
ClinVar
Risk rs431825413(C;C)
Alt rs431825413(C;C)
Reference rs431825413(;)
Significance Other
Disease Breast-ovarian cancer Pancreatic cancer Familial cancer of breast Hereditary breast and ovarian cancer syndrome Hereditary cancer-predisposing syndrome
Variation info
Gene BRCA1
CLNDBN Breast-ovarian cancer, familial 1 Pancreatic cancer, susceptibility to Familial cancer of breast Hereditary breast and ovarian cancer syndrome Hereditary cancer-predisposing syndrome
Reversed 1
HGVS NC_000017.10:g.41209082dupG
CLNSRC Breast Cancer Information Core (BRCA1) Inc. OMIM Allelic Variant
CLNACC RCV000019246.16, RCV000019247.3, RCV000056287.6, RCV000119097.6, RCV000131328.3,