Have questions? Visit https://www.reddit.com/r/SNPedia

rs786202251

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs786202251(-;-)
Make rs786202251(-;C)
ReferenceGRCh38.p2 38.2/146
Chromosome17
Position35101206
GeneRAD51D, RAD51L3-RFFL
is asnp
is mentioned by
dbSNPrs786202251
ebirs786202251
HLIrs786202251
Exacrs786202251
Varsomers786202251
Maprs786202251
PheGenIrs786202251
hapmaprs786202251
1000 genomesrs786202251
hgdprs786202251
ensemblrs786202251
gopubmedrs786202251
geneviewrs786202251
scholarrs786202251
googlers786202251
pharmgkbrs786202251
gwascentralrs786202251
openSNPrs786202251
23andMers786202251
23andMe allrs786202251
SNP Nexus

SNPshotrs786202251
SNPdbers786202251
MSV3drs786202251
GWAS Ctlgrs786202251
Max Magnitude0
ClinVar
Risk rs786202251(;)
Alt rs786202251(;)
Reference rs786202251(C;C)
Significance Probable-Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene RAD51D RAD51L3-RFFL
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 1
HGVS NC_000017.10:g.33428225delG
CLNSRC
CLNACC RCV000164969.1,