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rs189261858

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs189261858(A;A)
Make rs189261858(A;G)
ReferenceGRCh38.p7 38.3/149
Chromosome14
Position81143407
GeneLOC101928462, TSHR
is asnp
is mentioned by
dbSNPrs189261858
dbSNP (old)rs189261858
ClinGenrs189261858
ebirs189261858
HLIrs189261858
Exacrs189261858
Gnomadrs189261858
Varsomers189261858
Maprs189261858
PheGenIrs189261858
Biobankrs189261858
1000 genomesrs189261858
hgdprs189261858
ensemblrs189261858
gopubmedrs189261858
geneviewrs189261858
scholarrs189261858
googlers189261858
pharmgkbrs189261858
gwascentralrs189261858
openSNPrs189261858
23andMers189261858
23andMe allrs189261858
SNPshotrs189261858
SNPdbers189261858
MSV3drs189261858
GWAS Ctlgrs189261858
Max Magnitude0
ClinVar
Risk rs189261858(A;A)
Alt rs189261858(A;A)
Reference Rs189261858(G;G)
Significance Pathogenic
Disease not provided Hypothyroidism
Variation info
Gene LOC101928431 TSHR
CLNDBN not provided Hypothyroidism, congenital, nongoitrous, 1
Reversed 0
HGVS NC_000014.8:g.81609751G>A
CLNSRC
CLNACC RCV000273881.1, RCV000490528.1,