Rs121908863

From SNPedia
Jump to: navigation, search

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121908863(C;G)
Make rs121908863(G;G)
ReferenceGRCh38 38.1/141
Chromosome14
Position81092547
GeneLOC101928462, TSHR
is asnp
is mentioned by
dbSNPrs121908863
Exacrs121908863
PheGenIrs121908863
nextbiors121908863
hapmaprs121908863
1000 genomesrs121908863
hgdprs121908863
ensemblrs121908863
gopubmedrs121908863
geneviewrs121908863
scholarrs121908863
googlers121908863
pharmgkbrs121908863
gwascentralrs121908863
openSNPrs121908863
23andMers121908863
23andMe allrs121908863
SNP Nexus

SNPshotrs121908863
SNPdbers121908863
MSV3drs121908863
GMAF0.0009183
OMIM603372
Desc
Variant0006
Relatedalso
ClinVar
Risk rs121908863(G;G)
Alt rs121908863(G;G)
Reference rs121908863(C;C)
Significance Pathogenic
Disease Hypothyroidism
Variation info
Gene TSHR
CLNDBN Hypothyroidism, congenital, nongoitrous, 1
Reversed 0
HGVS NC_000014.8:g.81558891C>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000006805.1,