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rs17166050

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs17166050(C;T)
Make rs17166050(T;T)
ReferenceGRCh38 38.1/141
Chromosome5
Position132579521
GeneRAD50
is asnp
is mentioned by
dbSNPrs17166050
dbSNP (old)rs17166050
ClinGenrs17166050
ebirs17166050
HLIrs17166050
Exacrs17166050
Gnomadrs17166050
Varsomers17166050
Maprs17166050
PheGenIrs17166050
Biobankrs17166050
1000 genomesrs17166050
hgdprs17166050
ensemblrs17166050
gopubmedrs17166050
geneviewrs17166050
scholarrs17166050
googlers17166050
pharmgkbrs17166050
gwascentralrs17166050
openSNPrs17166050
23andMers17166050
23andMe allrs17166050
SNP Nexus

SNPshotrs17166050
SNPdbers17166050
MSV3drs17166050
GWAS Ctlgrs17166050
GMAF0.1676
Max Magnitude0
? (C;C) (C;T) (T;T) 28
[PMID 24093751OA-icon.png] Germline variants in MRE11/RAD50/NBN complex genes in childhood leukemia


[PMID 16724073] Sequence variation, linkage disequilibrium and association with Crohn's disease on chromosome 5q31.


[PMID 26014697] [Association between polymorphism of RAD50 gene and acute lymphoid leukemia in children]


ClinVar
Risk rs17166050(T;T)
Alt rs17166050(T;T)
Reference Rs17166050(C;C)
Significance Non-pathogenic
Disease not specified
Variation info
Gene RAD50
CLNDBN not specified
Reversed 1
HGVS NC_000005.9:g.131915213G>A
CLNSRC
CLNACC RCV000245201.1,