rs1060499695

Orientation

minus

Stabilized

minus

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

Make rs1060499695(A;G)

Make rs1060499695(G;G)

Reference

GRCh38.p7 38.3/150

Chromosome

3

Position

24127666

Gene

THRB

is a	snp
is	mentioned by
dbSNP	rs1060499695
dbSNP (classic)	rs1060499695
ClinGen	rs1060499695
ebi	rs1060499695
HLI	rs1060499695
Exac	rs1060499695
Gnomad	rs1060499695
Varsome	rs1060499695
LitVar	rs1060499695
Map	rs1060499695
PheGenI	rs1060499695
Biobank	rs1060499695
1000 genomes	rs1060499695
hgdp	rs1060499695
ensembl	rs1060499695
geneview	rs1060499695
scholar	rs1060499695
google	rs1060499695
pharmgkb	rs1060499695
gwascentral	rs1060499695
openSNP	rs1060499695
23andMe	rs1060499695
SNPshot	rs1060499695
SNPdbe	rs1060499695
MSV3d	rs1060499695
GWAS Ctlg	rs1060499695

Max Magnitude

0

ClinVar
Risk	rs1060499695(G;G)
Alt	rs1060499695(G;G)
Reference	Rs1060499695(A;A)
Significance	Probable-Pathogenic
Disease	Thyroid hormone resistance
Variation	info
Gene	THRB
CLNDBN	Thyroid hormone resistance, generalized, autosomal dominant
Reversed	1
HGVS	NC_000003.11:g.24169157T>C
CLNSRC
CLNACC	RCV000449629.1,