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rs104894023

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs104894023(C;T)
Make rs104894023(T;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position128254572
GeneLEP
is asnp
is mentioned by
dbSNPrs104894023
ebirs104894023
HLIrs104894023
Exacrs104894023
Varsomers104894023
Maprs104894023
PheGenIrs104894023
hapmaprs104894023
1000 genomesrs104894023
hgdprs104894023
ensemblrs104894023
gopubmedrs104894023
geneviewrs104894023
scholarrs104894023
googlers104894023
pharmgkbrs104894023
gwascentralrs104894023
openSNPrs104894023
23andMers104894023
23andMe allrs104894023
SNP Nexus

SNPshotrs104894023
SNPdbers104894023
MSV3drs104894023
GWAS Ctlgrs104894023
Max Magnitude0
OMIM164160
Desc
Variant0002
Relatedalso
ClinVar
Risk rs104894023(T;T)
Alt rs104894023(T;T)
Reference rs104894023(C;C)
Significance Pathogenic
Disease Leptin deficiency or dysfunction
Variation info
Gene LEP
CLNDBN Leptin deficiency or dysfunction
Reversed 0
HGVS NC_000007.13:g.127894625C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000015024.25,