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rs786203738

From SNPedia

Orientationplus
Geno Mag Summary
(CT;CT) 0 common in clinvar
Make rs786203738(-;-)
Make rs786203738(-;CT)
ReferenceGRCh38.p2 38.2/146
Chromosome5
Position132589655
GeneRAD50
is asnp
is mentioned by
dbSNPrs786203738
ebirs786203738
HLIrs786203738
Exacrs786203738
Varsomers786203738
Maprs786203738
PheGenIrs786203738
hapmaprs786203738
1000 genomesrs786203738
hgdprs786203738
ensemblrs786203738
gopubmedrs786203738
geneviewrs786203738
scholarrs786203738
googlers786203738
pharmgkbrs786203738
gwascentralrs786203738
openSNPrs786203738
23andMers786203738
23andMe allrs786203738
SNP Nexus

SNPshotrs786203738
SNPdbers786203738
MSV3drs786203738
GWAS Ctlgrs786203738
Max Magnitude0
ClinVar
Risk rs786203738(;)
Alt rs786203738(;)
Reference rs786203738(CT;CT)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene RAD50
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000005.9:g.131925347_131925348delCT
CLNSRC
CLNACC RCV000167173.4,