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rs773906955

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;G) 6 Ovarian cancer susceptibility
(G;G) 0 common in clinvar


Make rs773906955(A;A)
ReferenceGRCh38.p2 38.2/147
Chromosome17
Position35107026
GeneRAD51D, RAD51L3-RFFL
is asnp
is mentioned by
dbSNPrs773906955
dbSNP (classic)rs773906955
ClinGenrs773906955
ebirs773906955
HLIrs773906955
Exacrs773906955
Gnomadrs773906955
Varsomers773906955
LitVarrs773906955
Maprs773906955
PheGenIrs773906955
Biobankrs773906955
1000 genomesrs773906955
hgdprs773906955
ensemblrs773906955
geneviewrs773906955
scholarrs773906955
googlers773906955
pharmgkbrs773906955
gwascentralrs773906955
openSNPrs773906955
23andMers773906955
SNPshotrs773906955
SNPdbers773906955
MSV3drs773906955
GWAS Ctlgrs773906955
Max Magnitude6
ClinVar
Risk rs773906955(A;A)
Alt rs773906955(A;A)
Reference Rs773906955(G;G)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene RAD51D RAD51L3-RFFL
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000017.10:g.33434045G>A
CLNSRC
CLNACC RCV000215616.1,