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rs786201789

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs786201789(-;-)
Make rs786201789(-;C)
ReferenceGRCh38.p2 38.2/146
Chromosome5
Position132595805
GeneRAD50
is asnp
is mentioned by
dbSNPrs786201789
ebirs786201789
HLIrs786201789
Exacrs786201789
Varsomers786201789
Maprs786201789
PheGenIrs786201789
hapmaprs786201789
1000 genomesrs786201789
hgdprs786201789
ensemblrs786201789
gopubmedrs786201789
geneviewrs786201789
scholarrs786201789
googlers786201789
pharmgkbrs786201789
gwascentralrs786201789
openSNPrs786201789
23andMers786201789
23andMe allrs786201789
SNP Nexus

SNPshotrs786201789
SNPdbers786201789
MSV3drs786201789
GWAS Ctlgrs786201789
Max Magnitude0
ClinVar
Risk rs786201789(;)
Alt rs786201789(;)
Reference rs786201789(C;C)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene RAD50
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000005.9:g.131931497delC
CLNSRC
CLNACC RCV000164257.2,