rs121908871

Orientation

plus

Stabilized

plus

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

Make rs121908871(G;G)

Make rs121908871(G;T)

Reference

GRCh38 38.1/141

Chromosome

14

Position

81143228

Gene	LOC101928462, TSHR

is a	snp
is	mentioned by
dbSNP	rs121908871
dbSNP (classic)	rs121908871
ClinGen	rs121908871
ebi	rs121908871
HLI	rs121908871
Exac	rs121908871
Gnomad	rs121908871
Varsome	rs121908871
LitVar	rs121908871
Map	rs121908871
PheGenI	rs121908871
Biobank	rs121908871
1000 genomes	rs121908871
hgdp	rs121908871
ensembl	rs121908871
geneview	rs121908871
scholar	rs121908871
google	rs121908871
pharmgkb	rs121908871
gwascentral	rs121908871
openSNP	rs121908871
23andMe	rs121908871
SNPshot	rs121908871
SNPdbe	rs121908871
MSV3d	rs121908871
GWAS Ctlg	rs121908871

Max Magnitude

0

OMIM	603372
Desc
Variant	0015
Related	also

ClinVar
Risk	rs121908871(G;G)
Alt	rs121908871(G;G)
Reference	Rs121908871(T;T)
Significance	Pathogenic
Disease	Hypothyroidism
Variation	info
Gene	LOC101928431 TSHR
CLNDBN	Hypothyroidism, congenital, nongoitrous, 1
Reversed	0
HGVS	NC_000014.8:g.81609572T>G
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000006814.4,