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rs587780105

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs587780105(-;-)
Make rs587780105(-;C)
ReferenceGRCh38.p2 38.2/144
Chromosome17
Position35101356
GeneRAD51D, RAD51L3-RFFL
is asnp
is mentioned by
dbSNPrs587780105
ebirs587780105
HLIrs587780105
Exacrs587780105
Varsomers587780105
Maprs587780105
PheGenIrs587780105
hapmaprs587780105
1000 genomesrs587780105
hgdprs587780105
ensemblrs587780105
gopubmedrs587780105
geneviewrs587780105
scholarrs587780105
googlers587780105
pharmgkbrs587780105
gwascentralrs587780105
openSNPrs587780105
23andMers587780105
23andMe allrs587780105
SNP Nexus

SNPshotrs587780105
SNPdbers587780105
MSV3drs587780105
GWAS Ctlgrs587780105
Max Magnitude0
ClinVar
Risk rs587780105(;)
Alt rs587780105(;)
Reference rs587780105(C;C)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome not provided
Variation info
Gene RAD51D RAD51L3-RFFL
CLNDBN Hereditary cancer-predisposing syndrome not provided
Reversed 1
HGVS NC_000017.10:g.33428375delG
CLNSRC
CLNACC RCV000115820.5, RCV000212968.1,