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rs33997857

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common on affy axiom data
Make rs33997857(C;T)
Make rs33997857(T;T)
ReferenceGRCh38 38.1/142
Chromosome2
Position11787112
GeneLPIN1
is asnp
is mentioned by
dbSNPrs33997857
ebirs33997857
HLIrs33997857
Exacrs33997857
Varsomers33997857
Maprs33997857
PheGenIrs33997857
hapmaprs33997857
1000 genomesrs33997857
hgdprs33997857
ensemblrs33997857
gopubmedrs33997857
geneviewrs33997857
scholarrs33997857
googlers33997857
pharmgkbrs33997857
gwascentralrs33997857
openSNPrs33997857
23andMers33997857
23andMe allrs33997857
SNP Nexus

SNPshotrs33997857
SNPdbers33997857
MSV3drs33997857
GWAS Ctlgrs33997857
GMAF0.01102
Max Magnitude0

[PMID 20356931] Studies of association between LPIN1 variants and common metabolic phenotypes among 17,538 Danes

[PMID 18591397OA-icon.png] Evaluating the role of LPIN1 variation in insulin resistance, body weight, and human lipodystrophy in U.K. Populations.


GET Evidence
LPIN1-V494M
aa_change Val494Met
aa_change_short V494M
impact not reviewed
qualified_impact Insufficiently evaluated not reviewed
overall_frequency 0.016174
summary