rs17151919

plus

Geno	Mag	Summary
(G;G)	0	common in complete genomics

Make rs17151919(A;A)

Make rs17151919(A;G)

Reference

GRCh38 38.1/141

Chromosome

7

Position

128254539

Gene

LEP

is a	snp
is	mentioned by
dbSNP	rs17151919
dbSNP (classic)	rs17151919
ClinGen	rs17151919
ebi	rs17151919
HLI	rs17151919
Exac	rs17151919
Gnomad	rs17151919
Varsome	rs17151919
LitVar	rs17151919
Map	rs17151919
PheGenI	rs17151919
Biobank	rs17151919
1000 genomes	rs17151919
hgdp	rs17151919
ensembl	rs17151919
geneview	rs17151919
scholar	rs17151919
google	rs17151919
pharmgkb	rs17151919
gwascentral	rs17151919
openSNP	rs17151919
23andMe	rs17151919
SNPshot	rs17151919
SNPdbe	rs17151919
MSV3d	rs17151919
GWAS Ctlg	rs17151919

GMAF

0.0202

Max Magnitude

0

?

(A;A) (A;G) (G;G)

28

[PMID 20642810 ] Candidate molecular pathway genes related to appetite regulatory neural network, adipocyte homeostasis and obesity: results from the CARDIA Study

[PMID 18212354 ] Genes in glucose metabolism and association with spina bifida.

ClinVar
Risk	rs17151919(A;A)
Alt	rs17151919(A;A)
Reference	Rs17151919(G;G)
Significance	Probable-non-pathogenic
Disease	Monogenic Non-Syndromic Obesity Leptin deficiency or dysfunction Monogenic diabetes
Variation	info
Gene	LEP
CLNDBN	Monogenic Non-Syndromic Obesity Leptin deficiency or dysfunction Monogenic diabetes
Reversed	0
HGVS	NC_000007.13:g.127894592G>A
CLNSRC
CLNACC	RCV000306659.1, RCV000394361.1, RCV000445399.1,