rs28937584

Orientation

plus

Stabilized

plus

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

Make rs28937584(C;C)

Make rs28937584(C;G)

Reference

GRCh38 38.1/141

Chromosome

14

Position

81143955

Gene	LOC101928462, TSHR

is a	snp
is	mentioned by
dbSNP	rs28937584
dbSNP (classic)	rs28937584
ClinGen	rs28937584
ebi	rs28937584
HLI	rs28937584
Exac	rs28937584
Gnomad	rs28937584
Varsome	rs28937584
LitVar	rs28937584
Map	rs28937584
PheGenI	rs28937584
Biobank	rs28937584
1000 genomes	rs28937584
hgdp	rs28937584
ensembl	rs28937584
geneview	rs28937584
scholar	rs28937584
google	rs28937584
pharmgkb	rs28937584
gwascentral	rs28937584
openSNP	rs28937584
23andMe	rs28937584
SNPshot	rs28937584
SNPdbe	rs28937584
MSV3d	rs28937584
GWAS Ctlg	rs28937584

Max Magnitude

0

OMIM	603372
Desc	THYROID CARCINOMA WITH THYROTOXICOSIS
Variant	0008
Related	also

ClinVar
Risk	rs28937584(A;A) rs28937584(C;C)
Alt	rs28937584(A;A) rs28937584(C;C)
Reference	Rs28937584(G;G)
Significance	Pathogenic
Disease	THYROID CARCINOMA WITH THYROTOXICOSIS
Variation	info
Gene	LOC101928431 TSHR
CLNDBN	THYROID CARCINOMA WITH THYROTOXICOSIS, SOMATIC
Reversed	0
HGVS	NC_000014.8:g.81610299G>C
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000006807.3,