rs121908861

Orientation

plus

Stabilized

plus

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

Make rs121908861(C;C)

Make rs121908861(C;T)

Reference

GRCh38 38.1/141

Chromosome

14

Position

81143949

Gene	LOC101928462, TSHR

is a	snp
is	mentioned by
dbSNP	rs121908861
dbSNP (classic)	rs121908861
ClinGen	rs121908861
ebi	rs121908861
HLI	rs121908861
Exac	rs121908861
Gnomad	rs121908861
Varsome	rs121908861
LitVar	rs121908861
Map	rs121908861
PheGenI	rs121908861
Biobank	rs121908861
1000 genomes	rs121908861
hgdp	rs121908861
ensembl	rs121908861
geneview	rs121908861
scholar	rs121908861
google	rs121908861
pharmgkb	rs121908861
gwascentral	rs121908861
openSNP	rs121908861
23andMe	rs121908861
SNPshot	rs121908861
SNPdbe	rs121908861
MSV3d	rs121908861
GWAS Ctlg	rs121908861

Max Magnitude

0

OMIM	603372
Desc
Variant	0004
Related	also

ClinVar
Risk	rs121908861(C;C)
Alt	rs121908861(C;C)
Reference	Rs121908861(T;T)
Significance	Pathogenic
Disease	Hyperthyroidism Thyroid adenoma
Variation	info
Gene	LOC101928431 TSHR
CLNDBN	Hyperthyroidism, nonautoimmune Thyroid adenoma, hyperfunctioning
Reversed	0
HGVS	NC_000014.8:g.81610293T>C
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000006802.2, RCV000006803.4,