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rs724159998

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs724159998(G;T)
Make rs724159998(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome7
Position128254557
GeneLEP
is asnp
is mentioned by
dbSNPrs724159998
ebirs724159998
HLIrs724159998
Exacrs724159998
Varsomers724159998
Maprs724159998
PheGenIrs724159998
hapmaprs724159998
1000 genomesrs724159998
hgdprs724159998
ensemblrs724159998
gopubmedrs724159998
geneviewrs724159998
scholarrs724159998
googlers724159998
pharmgkbrs724159998
gwascentralrs724159998
openSNPrs724159998
23andMers724159998
23andMe allrs724159998
SNP Nexus

SNPshotrs724159998
SNPdbers724159998
MSV3drs724159998
GWAS Ctlgrs724159998
Max Magnitude0
ClinVar
Risk rs724159998(A,T;A,T)
Alt rs724159998(A,T;A,T)
Reference rs724159998(G;G)
Significance Pathogenic
Disease Leptin dysfunction
Variation info
Gene LEP
CLNDBN Leptin dysfunction
Reversed 0
HGVS NC_000007.13:g.127894610G>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000149807.3,