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rs71645922

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs71645922(A;A)
Make rs71645922(A;C)
ReferenceGRCh38 38.1/141
Chromosome3
Position45476581
GeneLARS2
is asnp
is mentioned by
dbSNPrs71645922
ebirs71645922
HLIrs71645922
Exacrs71645922
Varsomers71645922
Maprs71645922
PheGenIrs71645922
hapmaprs71645922
1000 genomesrs71645922
hgdprs71645922
ensemblrs71645922
gopubmedrs71645922
geneviewrs71645922
scholarrs71645922
googlers71645922
pharmgkbrs71645922
gwascentralrs71645922
openSNPrs71645922
23andMers71645922
23andMe allrs71645922
SNP Nexus

SNPshotrs71645922
SNPdbers71645922
MSV3drs71645922
GWAS Ctlgrs71645922
GMAF0.01561
Max Magnitude0
A 2009 study of 11,163 Dutch participants found no evidence to support previous data indicating a role for SNPs in this gene (LARS2) in type 2 diabetes susceptibility.[PMID 19847392OA-icon.png]


GET Evidence
LARS2-H324Q
aa_change His324Gln
aa_change_short H324Q
impact not reviewed
qualified_impact Insufficiently evaluated not reviewed
overall_frequency 0.0257483
summary



ClinVar
Risk rs71645922(A;A)
Alt rs71645922(A;A)
Reference rs71645922(C;C)
Significance Non-pathogenic
Disease not specified
Variation info
Gene LARS2
CLNDBN not specified
Reversed 0
HGVS NC_000003.11:g.45518073C>A
CLNSRC
CLNACC RCV000220287.1,