rs724159998

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(G;G)	0	common in clinvar

Make rs724159998(G;T)

Make rs724159998(T;T)

Reference

GRCh38.p2 38.2/144

Chromosome

7

Position

128254557

Gene

LEP

is a	snp
is	mentioned by
dbSNP	rs724159998
dbSNP (classic)	rs724159998
ClinGen	rs724159998
ebi	rs724159998
HLI	rs724159998
Exac	rs724159998
Gnomad	rs724159998
Varsome	rs724159998
LitVar	rs724159998
Map	rs724159998
PheGenI	rs724159998
Biobank	rs724159998
1000 genomes	rs724159998
hgdp	rs724159998
ensembl	rs724159998
geneview	rs724159998
scholar	rs724159998
google	rs724159998
pharmgkb	rs724159998
gwascentral	rs724159998
openSNP	rs724159998
23andMe	rs724159998
SNPshot	rs724159998
SNPdbe	rs724159998
MSV3d	rs724159998
GWAS Ctlg	rs724159998

Max Magnitude

0

ClinVar
Risk	rs724159998(A;A) rs724159998(T;T)
Alt	rs724159998(A;A) rs724159998(T;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,