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rs876659394

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs876659394(C;C)
Make rs876659394(C;T)
ReferenceGRCh38.p2 38.2/147
Chromosome17
Position35107364
GeneRAD51D, RAD51L3-RFFL
is asnp
is mentioned by
dbSNPrs876659394
ebirs876659394
HLIrs876659394
Exacrs876659394
Varsomers876659394
Maprs876659394
PheGenIrs876659394
hapmaprs876659394
1000 genomesrs876659394
hgdprs876659394
ensemblrs876659394
gopubmedrs876659394
geneviewrs876659394
scholarrs876659394
googlers876659394
pharmgkbrs876659394
gwascentralrs876659394
openSNPrs876659394
23andMers876659394
23andMe allrs876659394
SNP Nexus

SNPshotrs876659394
SNPdbers876659394
MSV3drs876659394
GWAS Ctlgrs876659394
Max Magnitude0
ClinVar
Risk rs876659394(C;C)
Alt rs876659394(C;C)
Reference rs876659394(T;T)
Significance Probable-Pathogenic
Disease Tumor susceptibility linked to germline BAP1 mutations Breast-ovarian cancer
Variation info
Gene RAD51D RAD51L3-RFFL
CLNDBN Tumor susceptibility linked to germline BAP1 mutations Breast-ovarian cancer, familial 4
Reversed 1
HGVS NC_000017.10:g.33434383A>G
CLNSRC
CLNACC RCV000214604.1, RCV000233270.1,