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rs1052501

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1052501(A;A)
Make rs1052501(A;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position41883906
GeneULK4
is asnp
is mentioned by
dbSNPrs1052501
dbSNP (old)rs1052501
ClinGenrs1052501
ebirs1052501
HLIrs1052501
Exacrs1052501
Gnomadrs1052501
Varsomers1052501
Maprs1052501
PheGenIrs1052501
Biobankrs1052501
1000 genomesrs1052501
hgdprs1052501
ensemblrs1052501
gopubmedrs1052501
geneviewrs1052501
scholarrs1052501
googlers1052501
pharmgkbrs1052501
gwascentralrs1052501
openSNPrs1052501
23andMers1052501
23andMe allrs1052501
SNPshotrs1052501
SNPdbers1052501
MSV3drs1052501
GWAS Ctlgrs1052501
GMAF0.2934
Max Magnitude0
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 22120009OA-icon.png]
Trait
Title Common variation at 3p22.1 and 7p15.3 influences multiple myeloma risk.
Risk Allele G
P-val 2E-8
Odds Ratio 1.3200 None



[PMID 24449210] Inherited genetic susceptibility to monoclonal gammopathy of unknown significance


[PMID 22945773OA-icon.png] Single-nucleotide polymorphism rs1052501 associated with monoclonal gammopathy of undetermined significance and multiple myeloma.


ClinVar
Risk rs1052501(A;A)
Alt rs1052501(A;A)
Reference Rs1052501(G;G)
Significance Non-pathogenic
Disease not specified
Variation info
Gene ULK4
CLNDBN not specified
Reversed 1
HGVS NC_000003.11:g.41925398C>T
CLNSRC
CLNACC RCV000454745.1,