Have questions? Visit https://www.reddit.com/r/SNPedia

rs794726988

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs794726988(C;T)
Make rs794726988(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome17
Position35100985
GeneRAD51D, RAD51L3-RFFL
is asnp
is mentioned by
dbSNPrs794726988
ebirs794726988
HLIrs794726988
Exacrs794726988
Varsomers794726988
Maprs794726988
PheGenIrs794726988
hapmaprs794726988
1000 genomesrs794726988
hgdprs794726988
ensemblrs794726988
gopubmedrs794726988
geneviewrs794726988
scholarrs794726988
googlers794726988
pharmgkbrs794726988
gwascentralrs794726988
openSNPrs794726988
23andMers794726988
23andMe allrs794726988
SNP Nexus

SNPshotrs794726988
SNPdbers794726988
MSV3drs794726988
GWAS Ctlgrs794726988
Max Magnitude0
ClinVar
Risk rs794726988(T;T)
Alt rs794726988(T;T)
Reference rs794726988(C;C)
Significance Other
Disease Breast-ovarian cancer
Variation info
Gene RAD51D RAD51L3-RFFL
CLNDBN Breast-ovarian cancer, familial 4
Reversed 1
HGVS NC_000017.10:g.33428004G>A
CLNSRC
CLNACC RCV000173764.2,