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rs794726988

From SNPedia

Orientationminus
Stabilizedminus
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
dbSNP (classic)rs794726988
ClinGenrs794726988
ebirs794726988
HLIrs794726988
Exacrs794726988
Gnomadrs794726988
Varsomers794726988
LitVarrs794726988
Maprs794726988
PheGenIrs794726988
Biobankrs794726988
1000 genomesrs794726988
hgdprs794726988
ensemblrs794726988
geneviewrs794726988
scholarrs794726988
googlers794726988
pharmgkbrs794726988
gwascentralrs794726988
openSNPrs794726988
23andMers794726988
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 not specified
Variation info
Gene RAD51D RAD51L3-RFFL
CLNDBN Breast-ovarian cancer, familial 4 not specified
Reversed 1
HGVS NC_000017.10:g.33428004G>A
CLNSRC
CLNACC RCV000173764.3, RCV000486976.1,