rs121908859

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(A;A)	0	common in complete genomics

Make rs121908859(A;G)

Make rs121908859(G;G)

Reference

GRCh38 38.1/141

Chromosome

14

Position

81143914

Gene	LOC101928462, TSHR

is a	snp
is	mentioned by
dbSNP	rs121908859
dbSNP (classic)	rs121908859
ClinGen	rs121908859
ebi	rs121908859
HLI	rs121908859
Exac	rs121908859
Gnomad	rs121908859
Varsome	rs121908859
LitVar	rs121908859
Map	rs121908859
PheGenI	rs121908859
Biobank	rs121908859
1000 genomes	rs121908859
hgdp	rs121908859
ensembl	rs121908859
geneview	rs121908859
scholar	rs121908859
google	rs121908859
pharmgkb	rs121908859
gwascentral	rs121908859
openSNP	rs121908859
23andMe	rs121908859
SNPshot	rs121908859
SNPdbe	rs121908859
MSV3d	rs121908859
GWAS Ctlg	rs121908859

Max Magnitude

0

OMIM	603372
Desc
Variant	0002
Related	also

ClinVar
Risk	rs121908859(G;G)
Alt	rs121908859(G;G)
Reference	Rs121908859(A;A)
Significance	Pathogenic
Disease	Thyroid adenoma
Variation	info
Gene	LOC101928431 TSHR
CLNDBN	Thyroid adenoma, hyperfunctioning
Reversed	0
HGVS	NC_000014.8:g.81610258A>G
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000006800.4,