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rs201889708

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs201889708(A;A)
Make rs201889708(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome14
Position81143400
GeneLOC101928462, TSHR
is asnp
is mentioned by
dbSNPrs201889708
ebirs201889708
HLIrs201889708
Exacrs201889708
Varsomers201889708
Maprs201889708
PheGenIrs201889708
hapmaprs201889708
1000 genomesrs201889708
hgdprs201889708
ensemblrs201889708
gopubmedrs201889708
geneviewrs201889708
scholarrs201889708
googlers201889708
pharmgkbrs201889708
gwascentralrs201889708
openSNPrs201889708
23andMers201889708
23andMe allrs201889708
SNP Nexus

SNPshotrs201889708
SNPdbers201889708
MSV3drs201889708
GWAS Ctlgrs201889708
Max Magnitude0
ClinVar
Risk rs201889708(A;A)
Alt rs201889708(A;A)
Reference rs201889708(G;G)
Significance Probable-Pathogenic
Disease Inborn genetic diseases
Variation info
Gene LOC101928431 TSHR
CLNDBN Inborn genetic diseases
Reversed 0
HGVS NC_000014.8:g.81609744G>A
CLNSRC
CLNACC RCV000190814.1,