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rs786203945

From SNPedia

Orientationplus
Geno Mag Summary
(CT;CT) 0 common in clinvar
Make rs786203945(-;-)
Make rs786203945(-;CT)
ReferenceGRCh38.p2 38.2/146
Chromosome17
Position58694966
GeneRAD51C
is asnp
is mentioned by
dbSNPrs786203945
ebirs786203945
HLIrs786203945
Exacrs786203945
Varsomers786203945
Maprs786203945
PheGenIrs786203945
hapmaprs786203945
1000 genomesrs786203945
hgdprs786203945
ensemblrs786203945
gopubmedrs786203945
geneviewrs786203945
scholarrs786203945
googlers786203945
pharmgkbrs786203945
gwascentralrs786203945
openSNPrs786203945
23andMers786203945
23andMe allrs786203945
SNP Nexus

SNPshotrs786203945
SNPdbers786203945
MSV3drs786203945
GWAS Ctlgrs786203945
Max Magnitude0
ClinVar
Risk rs786203945(;)
Alt rs786203945(;)
Reference rs786203945(CT;CT)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene RAD51C
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000017.10:g.56772327_56772328delCT
CLNSRC
CLNACC RCV000167466.1,