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rs431825365

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs431825365(-;-)
Make rs431825365(-;T)
ReferenceGRCh38 38.1/141
Chromosome13
Position32370533
GeneBRCA2
is asnp
is mentioned by
dbSNPrs431825365
ebirs431825365
HLIrs431825365
Exacrs431825365
Varsomers431825365
Maprs431825365
PheGenIrs431825365
hapmaprs431825365
1000 genomesrs431825365
hgdprs431825365
ensemblrs431825365
gopubmedrs431825365
geneviewrs431825365
scholarrs431825365
googlers431825365
pharmgkbrs431825365
gwascentralrs431825365
openSNPrs431825365
23andMers431825365
23andMe allrs431825365
SNP Nexus

SNPshotrs431825365
SNPdbers431825365
MSV3drs431825365
GWAS Ctlgrs431825365
Max Magnitude0
ClinVar
Risk rs431825365(;)
Alt rs431825365(;)
Reference rs431825365(T;T)
Significance Pathogenic
Disease Breast-ovarian cancer Hereditary breast and ovarian cancer syndrome
Variation info
Gene BRCA2
CLNDBN Breast-ovarian cancer, familial 2 Hereditary breast and ovarian cancer syndrome
Reversed 0
HGVS NC_000013.10:g.32944670delT
CLNSRC ClinVar
CLNACC RCV000082988.2, RCV000204425.2,