rs754658907

Orientation

plus

Stabilized

plus

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

Make rs754658907(C;T)

Make rs754658907(T;T)

Reference

GRCh38.p7 38.3/149

Chromosome

8

Position

132948928

Gene

TG

is a	snp
is	mentioned by
dbSNP	rs754658907
dbSNP (classic)	rs754658907
ClinGen	rs754658907
ebi	rs754658907
HLI	rs754658907
Exac	rs754658907
Gnomad	rs754658907
Varsome	rs754658907
LitVar	rs754658907
Map	rs754658907
PheGenI	rs754658907
Biobank	rs754658907
1000 genomes	rs754658907
hgdp	rs754658907
ensembl	rs754658907
geneview	rs754658907
scholar	rs754658907
google	rs754658907
pharmgkb	rs754658907
gwascentral	rs754658907
openSNP	rs754658907
23andMe	rs754658907
SNPshot	rs754658907
SNPdbe	rs754658907
MSV3d	rs754658907
GWAS Ctlg	rs754658907

Max Magnitude

0

ClinVar
Risk	rs754658907(T;T)
Alt	rs754658907(T;T)
Reference	Rs754658907(C;C)
Significance	Probable-Pathogenic
Disease	Thyroid dyshormonogenesis
Variation	info
Gene	TG
CLNDBN	Thyroid dyshormonogenesis
Reversed	0
HGVS	NC_000008.10:g.133961173C>T
CLNSRC	Illumina
CLNACC	RCV000363367.1,