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rs786202819

From SNPedia

Orientationminus
Geno Mag Summary
(AGGAACAGG;AGGAACAGG) 0 common in clinvar
Make rs786202819(-;-)
Make rs786202819(-;AGGAACAGG)
ReferenceGRCh38.p2 38.2/146
Chromosome17
Position35106987
GeneRAD51D, RAD51L3-RFFL
is asnp
is mentioned by
dbSNPrs786202819
ebirs786202819
HLIrs786202819
Exacrs786202819
Varsomers786202819
Maprs786202819
PheGenIrs786202819
hapmaprs786202819
1000 genomesrs786202819
hgdprs786202819
ensemblrs786202819
gopubmedrs786202819
geneviewrs786202819
scholarrs786202819
googlers786202819
pharmgkbrs786202819
gwascentralrs786202819
openSNPrs786202819
23andMers786202819
23andMe allrs786202819
SNP Nexus

SNPshotrs786202819
SNPdbers786202819
MSV3drs786202819
GWAS Ctlgrs786202819
Max Magnitude0
ClinVar
Risk rs786202819(;)
Alt rs786202819(;)
Reference rs786202819(AGGAACAGG;AGGAACAGG)
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.33434006_33434014delCCTGTTCCT
CLNSRC
CLNACC RCV000165835.1,