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

rs786202788

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs786202788(A;A)
Make rs786202788(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome17
Position35119531
GeneRAD51D, RAD51L3-RFFL
is asnp
is mentioned by
dbSNPrs786202788
ebirs786202788
HLIrs786202788
Exacrs786202788
Varsomers786202788
Maprs786202788
PheGenIrs786202788
hapmaprs786202788
1000 genomesrs786202788
hgdprs786202788
ensemblrs786202788
gopubmedrs786202788
geneviewrs786202788
scholarrs786202788
googlers786202788
pharmgkbrs786202788
gwascentralrs786202788
openSNPrs786202788
23andMers786202788
23andMe allrs786202788
SNP Nexus

SNPshotrs786202788
SNPdbers786202788
MSV3drs786202788
GWAS Ctlgrs786202788
Max Magnitude0
ClinVar
Risk rs786202788(A;A)
Alt rs786202788(A;A)
Reference rs786202788(G;G)
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.33446550C>T
CLNSRC
CLNACC RCV000165776.1,