rs121434633

Orientation

plus

Stabilized

plus

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

Make rs121434633(A;G)

Make rs121434633(G;G)

Reference

GRCh38 38.1/141

Chromosome

9

Position

84955510

Gene

NTRK2

is a	snp
is	mentioned by
dbSNP	rs121434633
dbSNP (classic)	rs121434633
ClinGen	rs121434633
ebi	rs121434633
HLI	rs121434633
Exac	rs121434633
Gnomad	rs121434633
Varsome	rs121434633
LitVar	rs121434633
Map	rs121434633
PheGenI	rs121434633
Biobank	rs121434633
1000 genomes	rs121434633
hgdp	rs121434633
ensembl	rs121434633
geneview	rs121434633
scholar	rs121434633
google	rs121434633
pharmgkb	rs121434633
gwascentral	rs121434633
openSNP	rs121434633
23andMe	rs121434633
SNPshot	rs121434633
SNPdbe	rs121434633
MSV3d	rs121434633
GWAS Ctlg	rs121434633

Max Magnitude

0

OMIM	600456
Desc
Variant	0001
Related	also

ClinVar
Risk	rs121434633(G;G)
Alt	rs121434633(G;G)
Reference	Rs121434633(A;A)
Significance	Pathogenic
Disease	Obesity
Variation	info
Gene	NTRK2
CLNDBN	Obesity, hyperphagia, and developmental delay
Reversed	0
HGVS	NC_000009.11:g.87570425A>G
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000009698.4,