rs786205080

Orientation

plus

Stabilized

plus

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

Make rs786205080(C;C)

Make rs786205080(C;G)

Reference

GRCh38.p2 38.2/146

Chromosome

14

Position

81092611

Gene	LOC101928462, TSHR

is a	snp
is	mentioned by
dbSNP	rs786205080
dbSNP (classic)	rs786205080
ClinGen	rs786205080
ebi	rs786205080
HLI	rs786205080
Exac	rs786205080
Gnomad	rs786205080
Varsome	rs786205080
LitVar	rs786205080
Map	rs786205080
PheGenI	rs786205080
Biobank	rs786205080
1000 genomes	rs786205080
hgdp	rs786205080
ensembl	rs786205080
geneview	rs786205080
scholar	rs786205080
google	rs786205080
pharmgkb	rs786205080
gwascentral	rs786205080
openSNP	rs786205080
23andMe	rs786205080
SNPshot	rs786205080
SNPdbe	rs786205080
MSV3d	rs786205080
GWAS Ctlg	rs786205080

Max Magnitude

0

ClinVar
Risk	rs786205080(C;C)
Alt	rs786205080(C;C)
Reference	Rs786205080(G;G)
Significance	Pathogenic
Disease	Hypothyroidism
Variation	info
Gene	LOC101928462 TSHR
CLNDBN	Hypothyroidism, congenital, nongoitrous, 1
Reversed	0
HGVS	NC_000014.8:g.81558955G>C
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000006832.4,