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rs374357106

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
(G;T) 6 Ovarian cancer susceptibility
Make rs374357106(A;A)
Make rs374357106(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome17
Position35118579
GeneRAD51D, RAD51L3-RFFL
is asnp
is mentioned by
dbSNPrs374357106
dbSNP (classic)rs374357106
ClinGenrs374357106
ebirs374357106
HLIrs374357106
Exacrs374357106
Gnomadrs374357106
Varsomers374357106
LitVarrs374357106
Maprs374357106
PheGenIrs374357106
Biobankrs374357106
1000 genomesrs374357106
hgdprs374357106
ensemblrs374357106
geneviewrs374357106
scholarrs374357106
googlers374357106
pharmgkbrs374357106
gwascentralrs374357106
openSNPrs374357106
23andMers374357106
SNPshotrs374357106
SNPdbers374357106
MSV3drs374357106
GWAS Ctlgrs374357106
Max Magnitude6
ClinVar
Risk rs374357106(A;A) rs374357106(C;C) rs374357106(T;T)
Alt rs374357106(A;A) rs374357106(C;C) rs374357106(T;T)
Reference Rs374357106(G;G)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome not specified Breast-ovarian cancer
Variation info
Gene RAD51D RAD51L3-RFFL
CLNDBN Hereditary cancer-predisposing syndrome not specified Breast-ovarian cancer, familial 4
Reversed 0
HGVS NC_000017.10:g.33445598G>A; NC_000017.10:g.33445598G>C; NC_000017.10:g.33445598G>T
CLNSRC
CLNACC RCV000164390.2, RCV000236527.2, RCV000461972.1, RCV000166932.1, RCV000467492.1,