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rs867328327

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs867328327(-;-)
Make rs867328327(-;A)
Make rs867328327(A;A)
ReferenceGRCh38.p2 38.2/147
Chromosome5
Position132557417
GeneIL5, RAD50
is asnp
is mentioned by
dbSNPrs867328327
ebirs867328327
HLIrs867328327
Exacrs867328327
Varsomers867328327
Maprs867328327
PheGenIrs867328327
hapmaprs867328327
1000 genomesrs867328327
hgdprs867328327
ensemblrs867328327
gopubmedrs867328327
geneviewrs867328327
scholarrs867328327
googlers867328327
pharmgkbrs867328327
gwascentralrs867328327
openSNPrs867328327
23andMers867328327
23andMe allrs867328327
SNP Nexus

SNPshotrs867328327
SNPdbers867328327
MSV3drs867328327
GWAS Ctlgrs867328327
Max Magnitude0
ClinVar
Risk rs867328327(A;A)
Alt rs867328327(A;A)
Reference rs867328327(;)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene RAD50 IL5
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000005.9:g.131893110dupA
CLNSRC
CLNACC RCV000129727.3,