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rs786203403

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs786203403(-;-)
Make rs786203403(-;T)
ReferenceGRCh38.p2 38.2/146
Chromosome5
Position132588003
GeneRAD50
is asnp
is mentioned by
dbSNPrs786203403
ebirs786203403
HLIrs786203403
Exacrs786203403
Varsomers786203403
Maprs786203403
PheGenIrs786203403
hapmaprs786203403
1000 genomesrs786203403
hgdprs786203403
ensemblrs786203403
gopubmedrs786203403
geneviewrs786203403
scholarrs786203403
googlers786203403
pharmgkbrs786203403
gwascentralrs786203403
openSNPrs786203403
23andMers786203403
23andMe allrs786203403
SNP Nexus

SNPshotrs786203403
SNPdbers786203403
MSV3drs786203403
GWAS Ctlgrs786203403
Max Magnitude0
ClinVar
Risk rs786203403(;)
Alt rs786203403(;)
Reference rs786203403(T;T)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene RAD50
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000005.9:g.131923695delT
CLNSRC
CLNACC RCV000166691.1,