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rs786203137

From SNPedia

Orientationminus
Geno Mag Summary
(GT;GT) 0 common in clinvar
Make rs786203137(-;-)
Make rs786203137(-;GT)
ReferenceGRCh38.p2 38.2/146
Chromosome17
Position35119160
GeneRAD51D, RAD51L3-RFFL
is asnp
is mentioned by
dbSNPrs786203137
ebirs786203137
HLIrs786203137
Exacrs786203137
Varsomers786203137
Maprs786203137
PheGenIrs786203137
hapmaprs786203137
1000 genomesrs786203137
hgdprs786203137
ensemblrs786203137
gopubmedrs786203137
geneviewrs786203137
scholarrs786203137
googlers786203137
pharmgkbrs786203137
gwascentralrs786203137
openSNPrs786203137
23andMers786203137
23andMe allrs786203137
SNP Nexus

SNPshotrs786203137
SNPdbers786203137
MSV3drs786203137
GWAS Ctlgrs786203137
Max Magnitude0
ClinVar
Risk rs786203137(;)
Alt rs786203137(;)
Reference rs786203137(GT;GT)
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.33446179_33446180delAC
CLNSRC
CLNACC RCV000166313.1,