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rs587781756

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs587781756(C;T)
Make rs587781756(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome17
Position35107017
GeneRAD51D, RAD51L3-RFFL
is asnp
is mentioned by
dbSNPrs587781756
ebirs587781756
HLIrs587781756
Exacrs587781756
Varsomers587781756
Maprs587781756
PheGenIrs587781756
hapmaprs587781756
1000 genomesrs587781756
hgdprs587781756
ensemblrs587781756
gopubmedrs587781756
geneviewrs587781756
scholarrs587781756
googlers587781756
pharmgkbrs587781756
gwascentralrs587781756
openSNPrs587781756
23andMers587781756
23andMe allrs587781756
SNP Nexus

SNPshotrs587781756
SNPdbers587781756
MSV3drs587781756
GWAS Ctlgrs587781756
Max Magnitude0
ClinVar
Risk rs587781756(T;T)
Alt rs587781756(T;T)
Reference rs587781756(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.33434036G>A
CLNSRC
CLNACC RCV000129970.2,