rs137854434

Orientation

plus

Stabilized

plus

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

Make rs137854434(A;A)

Make rs137854434(A;G)

Reference

GRCh38 38.1/141

Chromosome

8

Position

133029907

Gene

TG

is a	snp
is	mentioned by
dbSNP	rs137854434
dbSNP (classic)	rs137854434
ClinGen	rs137854434
ebi	rs137854434
HLI	rs137854434
Exac	rs137854434
Gnomad	rs137854434
Varsome	rs137854434
LitVar	rs137854434
Map	rs137854434
PheGenI	rs137854434
Biobank	rs137854434
1000 genomes	rs137854434
hgdp	rs137854434
ensembl	rs137854434
geneview	rs137854434
scholar	rs137854434
google	rs137854434
pharmgkb	rs137854434
gwascentral	rs137854434
openSNP	rs137854434
23andMe	rs137854434
SNPshot	rs137854434
SNPdbe	rs137854434
MSV3d	rs137854434
GWAS Ctlg	rs137854434

Max Magnitude

0

OMIM	188450
Desc
Variant	0015
Related	also

ClinVar
Risk	rs137854434(A;A)
Alt	rs137854434(A;A)
Reference	Rs137854434(G;G)
Significance	Pathogenic
Disease	Iodotyrosyl coupling defect
Variation	info
Gene	TG
CLNDBN	Iodotyrosyl coupling defect
Reversed	0
HGVS	NC_000008.10:g.134042152G>A
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000013540.24,