rs121909065

Orientation

plus

Stabilized

plus

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

Make rs121909065(C;C)

Make rs121909065(C;G)

Reference

GRCh38 38.1/141

Chromosome

5

Position

71719903

Gene

CARTPT

is a	snp
is	mentioned by
dbSNP	rs121909065
dbSNP (classic)	rs121909065
ClinGen	rs121909065
ebi	rs121909065
HLI	rs121909065
Exac	rs121909065
Gnomad	rs121909065
Varsome	rs121909065
LitVar	rs121909065
Map	rs121909065
PheGenI	rs121909065
Biobank	rs121909065
1000 genomes	rs121909065
hgdp	rs121909065
ensembl	rs121909065
geneview	rs121909065
scholar	rs121909065
google	rs121909065
pharmgkb	rs121909065
gwascentral	rs121909065
openSNP	rs121909065
23andMe	rs121909065
SNPshot	rs121909065
SNPdbe	rs121909065
MSV3d	rs121909065
GWAS Ctlg	rs121909065

Max Magnitude

0

OMIM	602606
Desc
Variant	0001
Related	also

ClinVar
Risk	rs121909065(C;C)
Alt	rs121909065(C;C)
Reference	Rs121909065(G;G)
Significance	Other
Disease	Obesity
Variation	info
Gene	CARTPT
CLNDBN	Obesity
Reversed	0
HGVS	NC_000005.9:g.71015730G>C
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000023199.3,