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rs760146707

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs760146707(-;-)
Make rs760146707(-;T)
ReferenceGRCh38.p2 38.2/144
Chromosome5
Position132579997
GeneRAD50
is asnp
is mentioned by
dbSNPrs760146707
ebirs760146707
HLIrs760146707
Exacrs760146707
Varsomers760146707
Maprs760146707
PheGenIrs760146707
hapmaprs760146707
1000 genomesrs760146707
hgdprs760146707
ensemblrs760146707
gopubmedrs760146707
geneviewrs760146707
scholarrs760146707
googlers760146707
pharmgkbrs760146707
gwascentralrs760146707
openSNPrs760146707
23andMers760146707
23andMe allrs760146707
SNP Nexus

SNPshotrs760146707
SNPdbers760146707
MSV3drs760146707
GWAS Ctlgrs760146707
Max Magnitude0
ClinVar
Risk rs760146707(;)
Alt rs760146707(;)
Reference rs760146707(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.131915689delT
CLNSRC
CLNACC RCV000164362.1,