Have questions? Visit https://www.reddit.com/r/SNPedia

rs28937584

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs28937584(C;C)
Make rs28937584(C;G)
ReferenceGRCh38 38.1/141
Chromosome14
Position81143955
GeneLOC101928431, TSHR
is asnp
is mentioned by
dbSNPrs28937584
ebirs28937584
HLIrs28937584
Exacrs28937584
Varsomers28937584
Maprs28937584
PheGenIrs28937584
hapmaprs28937584
1000 genomesrs28937584
hgdprs28937584
ensemblrs28937584
gopubmedrs28937584
geneviewrs28937584
scholarrs28937584
googlers28937584
pharmgkbrs28937584
gwascentralrs28937584
openSNPrs28937584
23andMers28937584
23andMe allrs28937584
SNP Nexus

SNPshotrs28937584
SNPdbers28937584
MSV3drs28937584
GWAS Ctlgrs28937584
Max Magnitude0
OMIM603372
DescTHYROID CARCINOMA WITH THYROTOXICOSIS
Variant0008
Relatedalso
Neighborrs1991517
Distance284


ClinVar
Risk rs28937584(C;C)
Alt 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,