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rs786202750

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs786202750(-;-)
Make rs786202750(-;T)
ReferenceGRCh38.p2 38.2/146
Chromosome17
Position35106398
GeneRAD51D, RAD51L3-RFFL
is asnp
is mentioned by
dbSNPrs786202750
ebirs786202750
HLIrs786202750
Exacrs786202750
Varsomers786202750
Maprs786202750
PheGenIrs786202750
hapmaprs786202750
1000 genomesrs786202750
hgdprs786202750
ensemblrs786202750
gopubmedrs786202750
geneviewrs786202750
scholarrs786202750
googlers786202750
pharmgkbrs786202750
gwascentralrs786202750
openSNPrs786202750
23andMers786202750
23andMe allrs786202750
SNP Nexus

SNPshotrs786202750
SNPdbers786202750
MSV3drs786202750
GWAS Ctlgrs786202750
Max Magnitude0
ClinVar
Risk rs786202750(;)
Alt rs786202750(;)
Reference rs786202750(T;T)
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.33433417delA
CLNSRC
CLNACC RCV000165722.1,