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rs10954174

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
(G;G) 0 common in complete genomics
Make rs10954174(A;G)
ReferenceGRCh38 38.1/141
Chromosome7
Position128256483
GeneLEP
is asnp
is mentioned by
dbSNPrs10954174
dbSNP (classic)rs10954174
ClinGenrs10954174
ebirs10954174
HLIrs10954174
Exacrs10954174
Gnomadrs10954174
Varsomers10954174
LitVarrs10954174
Maprs10954174
PheGenIrs10954174
Biobankrs10954174
1000 genomesrs10954174
hgdprs10954174
ensemblrs10954174
geneviewrs10954174
scholarrs10954174
googlers10954174
pharmgkbrs10954174
gwascentralrs10954174
openSNPrs10954174
23andMers10954174
SNPshotrs10954174
SNPdbers10954174
MSV3drs10954174
GWAS Ctlgrs10954174
GMAF0.03673
Max Magnitude0
? (A;A) (A;G) (G;G) 28


[PMID 19562039OA-icon.png] Targeting 160 candidate genes for blood pressure regulation with a genome-wide genotyping array


[PMID 22615788OA-icon.png] Normal Leptin Expression, Lower Adipogenic Ability, Decreased Leptin Receptor and Hyposensitivity to Leptin in Adolescent Idiopathic Scoliosis


[PMID 22614171OA-icon.png] Appetite regulation genes are associated with body mass index in black South African adolescents: a genetic association study.


ClinVar
Risk Rs10954174(G;G)
Alt Rs10954174(G;G)
Reference Rs10954174(A;A)
Significance Non-pathogenic
Disease Leptin deficiency or dysfunction Monogenic Non-Syndromic Obesity
Variation info
Gene LEP
CLNDBN Leptin deficiency or dysfunction Monogenic Non-Syndromic Obesity
Reversed 0
HGVS NC_000007.13:g.127896536A>G
CLNSRC
CLNACC RCV000279850.1, RCV000404055.1,