rs772490052

Orientation

plus

Stabilized

plus

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

Make rs772490052(C;T)

Make rs772490052(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

14

Position

81143581

Gene	LOC101928462, TSHR

is a	snp
is	mentioned by
dbSNP	rs772490052
dbSNP (classic)	rs772490052
ClinGen	rs772490052
ebi	rs772490052
HLI	rs772490052
Exac	rs772490052
Gnomad	rs772490052
Varsome	rs772490052
LitVar	rs772490052
Map	rs772490052
PheGenI	rs772490052
Biobank	rs772490052
1000 genomes	rs772490052
hgdp	rs772490052
ensembl	rs772490052
geneview	rs772490052
scholar	rs772490052
google	rs772490052
pharmgkb	rs772490052
gwascentral	rs772490052
openSNP	rs772490052
23andMe	rs772490052
SNPshot	rs772490052
SNPdbe	rs772490052
MSV3d	rs772490052
GWAS Ctlg	rs772490052

Max Magnitude

0

ClinVar
Risk	rs772490052(T;T)
Alt	rs772490052(T;T)
Reference	Rs772490052(C;C)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	LOC101928431 TSHR
CLNDBN	not provided
Reversed	0
HGVS	NC_000014.8:g.81609925C>T
CLNSRC
CLNACC	RCV000487167.1,