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rs587782695

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs587782695(C;T)
Make rs587782695(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome17
Position35106415
GeneRAD51D, RAD51L3-RFFL
is asnp
is mentioned by
dbSNPrs587782695
ebirs587782695
HLIrs587782695
Exacrs587782695
Varsomers587782695
Maprs587782695
PheGenIrs587782695
hapmaprs587782695
1000 genomesrs587782695
hgdprs587782695
ensemblrs587782695
gopubmedrs587782695
geneviewrs587782695
scholarrs587782695
googlers587782695
pharmgkbrs587782695
gwascentralrs587782695
openSNPrs587782695
23andMers587782695
23andMe allrs587782695
SNP Nexus

SNPshotrs587782695
SNPdbers587782695
MSV3drs587782695
GWAS Ctlgrs587782695
Max Magnitude0
ClinVar
Risk rs587782695(T;T)
Alt rs587782695(T;T)
Reference rs587782695(C;C)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene RAD51D RAD51L3-RFFL
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 1
HGVS NC_000017.10:g.33433434G>A
CLNSRC
CLNACC RCV000132135.2,