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rs119489103

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs119489103(A;A)
Make rs119489103(A;G)
ReferenceGRCh38 38.1/141
Chromosome11
Position45898159
GeneMAPK8IP1
is asnp
is mentioned by
dbSNPrs119489103
ebirs119489103
HLIrs119489103
Exacrs119489103
Varsomers119489103
Maprs119489103
PheGenIrs119489103
hapmaprs119489103
1000 genomesrs119489103
hgdprs119489103
ensemblrs119489103
gopubmedrs119489103
geneviewrs119489103
scholarrs119489103
googlers119489103
pharmgkbrs119489103
gwascentralrs119489103
openSNPrs119489103
23andMers119489103
23andMe allrs119489103
SNP Nexus

SNPshotrs119489103
SNPdbers119489103
MSV3drs119489103
GWAS Ctlgrs119489103
Max Magnitude0
OMIM604641
Desc
Variant0001
Relatedalso
ClinVar
Risk rs119489103(A;A)
Alt rs119489103(A;A)
Reference rs119489103(G;G)
Significance Pathogenic
Disease Diabetes mellitus type 2
Variation info
Gene MAPK8IP1
CLNDBN Diabetes mellitus type 2
Reversed 0
HGVS NC_000011.9:g.45919710G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000005752.2,