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rs786203805

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs786203805(A;A)
Make rs786203805(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome5
Position132616131
GeneRAD50
is asnp
is mentioned by
dbSNPrs786203805
ebirs786203805
HLIrs786203805
Exacrs786203805
Varsomers786203805
Maprs786203805
PheGenIrs786203805
hapmaprs786203805
1000 genomesrs786203805
hgdprs786203805
ensemblrs786203805
gopubmedrs786203805
geneviewrs786203805
scholarrs786203805
googlers786203805
pharmgkbrs786203805
gwascentralrs786203805
openSNPrs786203805
23andMers786203805
23andMe allrs786203805
SNP Nexus

SNPshotrs786203805
SNPdbers786203805
MSV3drs786203805
GWAS Ctlgrs786203805
Max Magnitude0
ClinVar
Risk rs786203805(A,T;A,T)
Alt rs786203805(A,T;A,T)
Reference rs786203805(G;G)
Significance Probable-Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene RAD50
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000005.9:g.131951823G>A; NC_000005.9:g.131951823G>T
CLNSRC
CLNACC RCV000167267.1, RCV000167343.1,