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rs7144481

From SNPedia

Orientationplus
Stabilizedplus
Make rs7144481(C;C)
Make rs7144481(C;T)
Make rs7144481(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome14
Position81144598
GeneLOC101928462, TSHR
is asnp
is mentioned by
dbSNPrs7144481
ClinGenrs7144481
ebirs7144481
HLIrs7144481
Exacrs7144481
Varsomers7144481
Maprs7144481
PheGenIrs7144481
hapmaprs7144481
1000 genomesrs7144481
hgdprs7144481
ensemblrs7144481
gopubmedrs7144481
geneviewrs7144481
scholarrs7144481
googlers7144481
pharmgkbrs7144481
gwascentralrs7144481
openSNPrs7144481
23andMers7144481
23andMe allrs7144481
SNP Nexus

SNPshotrs7144481
SNPdbers7144481
MSV3drs7144481
GWAS Ctlgrs7144481
Max Magnitude
? (C;C) (C;T) (T;T) 28
[PMID 26231489] Current Progress in Sports Genomics


ClinVar
Risk rs7144481(T;T)
Alt rs7144481(T;T)
Reference rs7144481(C;C)
Significance Probable-non-pathogenic
Disease Hyperthyroidism Congenital hypothyroidism
Variation info
Gene LOC101928431 TSHR
CLNDBN Hyperthyroidism, nonautoimmune Congenital hypothyroidism
Reversed 0
HGVS NC_000014.8:g.81610942C>T
CLNSRC
CLNACC RCV000340818.1, RCV000398726.1,