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rs377260382

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs377260382(A;A)
Make rs377260382(A;G)
ReferenceGRCh38 38.1/142
Chromosome5
Position132557327
GeneIL5, RAD50
is asnp
is mentioned by
dbSNPrs377260382
ebirs377260382
HLIrs377260382
Exacrs377260382
Varsomers377260382
Maprs377260382
PheGenIrs377260382
hapmaprs377260382
1000 genomesrs377260382
hgdprs377260382
ensemblrs377260382
gopubmedrs377260382
geneviewrs377260382
scholarrs377260382
googlers377260382
pharmgkbrs377260382
gwascentralrs377260382
openSNPrs377260382
23andMers377260382
23andMe allrs377260382
SNP Nexus

SNPshotrs377260382
SNPdbers377260382
MSV3drs377260382
GWAS Ctlgrs377260382
Max Magnitude0
ClinVar
Risk rs377260382(A;A)
Alt rs377260382(A;A)
Reference rs377260382(G;G)
Significance Other
Disease Hereditary cancer-predisposing syndrome not provided
Variation info
Gene RAD50 IL5
CLNDBN Hereditary cancer-predisposing syndrome not provided
Reversed 0
HGVS NC_000005.9:g.131893019G>A
CLNSRC Ambry Genetics ClinVar GeneDx
CLNACC RCV000115961.8, RCV000212899.1,