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rs1800571

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1800571(A;A)
Make rs1800571(A;C)
ReferenceGRCh38 38.1/141
Chromosome3
Position12381349
GenePPARG
is asnp
is mentioned by
dbSNPrs1800571
ebirs1800571
HLIrs1800571
Exacrs1800571
Varsomers1800571
Maprs1800571
PheGenIrs1800571
hapmaprs1800571
1000 genomesrs1800571
hgdprs1800571
ensemblrs1800571
gopubmedrs1800571
geneviewrs1800571
scholarrs1800571
googlers1800571
pharmgkbrs1800571
gwascentralrs1800571
openSNPrs1800571
23andMers1800571
23andMe allrs1800571
SNP Nexus

SNPshotrs1800571
SNPdbers1800571
MSV3drs1800571
GWAS Ctlgrs1800571
Max Magnitude0
OMIM601487
Desc
Variant0001
Relatedalso


ClinVar
Risk rs1800571(A;A)
Alt rs1800571(A;A)
Reference rs1800571(C;C)
Significance Pathogenic
Disease Morbid obesity
Variation info
Gene PPARG
CLNDBN Morbid obesity
Reversed 0
HGVS NC_000003.11:g.12422848C>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000008603.3,



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