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rs121909065

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in complete genomics
Make rs121909065(C;C)
Make rs121909065(C;G)
ReferenceGRCh38 38.1/141
Chromosome5
Position71719903
GeneCARTPT
is asnp
is mentioned by
dbSNPrs121909065
ebirs121909065
HLIrs121909065
Exacrs121909065
Varsomers121909065
Maprs121909065
PheGenIrs121909065
hapmaprs121909065
1000 genomesrs121909065
hgdprs121909065
ensemblrs121909065
gopubmedrs121909065
geneviewrs121909065
scholarrs121909065
googlers121909065
pharmgkbrs121909065
gwascentralrs121909065
openSNPrs121909065
23andMers121909065
23andMe allrs121909065
SNP Nexus

SNPshotrs121909065
SNPdbers121909065
MSV3drs121909065
GWAS Ctlgrs121909065
Max Magnitude0
OMIM602606
Desc
Variant0001
Relatedalso
ClinVar
Risk rs121909065(C;C)
Alt rs121909065(C;C)
Reference rs121909065(G;G)
Significance Other
Disease Obesity
Variation info
Gene CARTPT
CLNDBN Obesity
Reversed 0
HGVS NC_000005.9:g.71015730G>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000023199.3,