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rs587782736

From SNPedia

Orientationminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs587782736(-;-)
Make rs587782736(-;AA)
Make rs587782736(AA;AA)
ReferenceGRCh38.p2 38.2/144
Chromosome17
Position35119114
GeneRAD51D, RAD51L3-RFFL
is asnp
is mentioned by
dbSNPrs587782736
ebirs587782736
HLIrs587782736
Exacrs587782736
Varsomers587782736
Maprs587782736
PheGenIrs587782736
hapmaprs587782736
1000 genomesrs587782736
hgdprs587782736
ensemblrs587782736
gopubmedrs587782736
geneviewrs587782736
scholarrs587782736
googlers587782736
pharmgkbrs587782736
gwascentralrs587782736
openSNPrs587782736
23andMers587782736
23andMe allrs587782736
SNP Nexus

SNPshotrs587782736
SNPdbers587782736
MSV3drs587782736
GWAS Ctlgrs587782736
Max Magnitude0
ClinVar
Risk rs587782736(AA;AA)
Alt rs587782736(AA;AA)
Reference rs587782736(;)
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.33446133_33446134insTT
CLNSRC
CLNACC RCV000132237.2,