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rs587780104

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs587780104(C;T)
Make rs587780104(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome17
Position35103298
GeneRAD51D, RAD51L3-RFFL
is asnp
is mentioned by
dbSNPrs587780104
ebirs587780104
HLIrs587780104
Exacrs587780104
Varsomers587780104
Maprs587780104
PheGenIrs587780104
hapmaprs587780104
1000 genomesrs587780104
hgdprs587780104
ensemblrs587780104
gopubmedrs587780104
geneviewrs587780104
scholarrs587780104
googlers587780104
pharmgkbrs587780104
gwascentralrs587780104
openSNPrs587780104
23andMers587780104
23andMe allrs587780104
SNP Nexus

SNPshotrs587780104
SNPdbers587780104
MSV3drs587780104
GWAS Ctlgrs587780104
Max Magnitude0
ClinVar
Risk rs587780104(T;T)
Alt rs587780104(T;T)
Reference rs587780104(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.33430317G>A
CLNSRC Inc.
CLNACC RCV000115819.6, RCV000212965.1,