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rs786202179

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(CGGCTTTCCCCGTGAA;CGGCTTTCCCCGTGAA) 0 common in clinvar
Make rs786202179(-;-)
Make rs786202179(-;CGGCTTTCCCCGTGAA)
ReferenceGRCh38.p2 38.2/146
Chromosome17
Position35118564
GeneRAD51D, RAD51L3-RFFL
is asnp
is mentioned by
dbSNPrs786202179
dbSNP (old)rs786202179
ClinGenrs786202179
ebirs786202179
HLIrs786202179
Exacrs786202179
Varsomers786202179
Maprs786202179
PheGenIrs786202179
Biobankrs786202179
1000 genomesrs786202179
hgdprs786202179
ensemblrs786202179
gopubmedrs786202179
geneviewrs786202179
scholarrs786202179
googlers786202179
pharmgkbrs786202179
gwascentralrs786202179
openSNPrs786202179
23andMers786202179
23andMe allrs786202179
SNP Nexus

SNPshotrs786202179
SNPdbers786202179
MSV3drs786202179
GWAS Ctlgrs786202179
Max Magnitude0
ClinVar
Risk rs786202179(-;-)
Alt rs786202179(-;-)
Reference Rs786202179(CGGCTTTCCCCGTGAA;CGGCTTTCCCCGTGAA)
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.33445583_33445598del16
CLNSRC
CLNACC RCV000164875.1,