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rs786202434

From SNPedia

Orientationminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs786202434(-;-)
Make rs786202434(-;T)
Make rs786202434(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome17
Position35107380
GeneRAD51D, RAD51L3-RFFL
is asnp
is mentioned by
dbSNPrs786202434
ebirs786202434
HLIrs786202434
Exacrs786202434
Varsomers786202434
Maprs786202434
PheGenIrs786202434
hapmaprs786202434
1000 genomesrs786202434
hgdprs786202434
ensemblrs786202434
gopubmedrs786202434
geneviewrs786202434
scholarrs786202434
googlers786202434
pharmgkbrs786202434
gwascentralrs786202434
openSNPrs786202434
23andMers786202434
23andMe allrs786202434
SNP Nexus

SNPshotrs786202434
SNPdbers786202434
MSV3drs786202434
GWAS Ctlgrs786202434
Max Magnitude0
ClinVar
Risk rs786202434(T;T)
Alt rs786202434(T;T)
Reference rs786202434(;)
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.33434400dupA
CLNSRC
CLNACC RCV000165244.1,