rs121908860

Orientation

plus

Stabilized

plus

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

Make rs121908860(AT;AT)

Make rs121908860(AT;GC)

Reference

GRCh38 38.1/141

Chromosome

14

Position

81143925

Gene	LOC101928462, TSHR

is a	snp
is	mentioned by
dbSNP	rs121908860
dbSNP (classic)	rs121908860
ClinGen	rs121908860
ebi	rs121908860
HLI	rs121908860
Exac	rs121908860
Gnomad	rs121908860
Varsome	rs121908860
LitVar	rs121908860
Map	rs121908860
PheGenI	rs121908860
Biobank	rs121908860
1000 genomes	rs121908860
hgdp	rs121908860
ensembl	rs121908860
geneview	rs121908860
scholar	rs121908860
google	rs121908860
pharmgkb	rs121908860
gwascentral	rs121908860
openSNP	rs121908860
23andMe	rs121908860
SNPshot	rs121908860
SNPdbe	rs121908860
MSV3d	rs121908860
GWAS Ctlg	rs121908860

Max Magnitude

0

OMIM	603372
Desc
Variant	0003
Related	also

ClinVar
Risk	rs121908860(AT;AT)
Alt	rs121908860(AT;AT)
Reference	Rs121908860(GC;GC)
Significance	Pathogenic
Disease	Thyroid adenoma
Variation	info
Gene	LOC101928431 TSHR
CLNDBN	Thyroid adenoma, hyperfunctioning
Reversed	0
HGVS	NC_000014.8:g.81610269_81610270delGCinsAT
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000006801.5,