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rs121909177

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121909177(C;G)
Make rs121909177(G;G)
ReferenceGRCh38 38.1/141
Chromosome19
Position17888397
GeneSLC5A5
is asnp
is mentioned by
dbSNPrs121909177
ebirs121909177
HLIrs121909177
Exacrs121909177
Varsomers121909177
Maprs121909177
PheGenIrs121909177
hapmaprs121909177
1000 genomesrs121909177
hgdprs121909177
ensemblrs121909177
gopubmedrs121909177
geneviewrs121909177
scholarrs121909177
googlers121909177
pharmgkbrs121909177
gwascentralrs121909177
openSNPrs121909177
23andMers121909177
23andMe allrs121909177
SNP Nexus

SNPshotrs121909177
SNPdbers121909177
MSV3drs121909177
GWAS Ctlgrs121909177
Max Magnitude0
OMIM601843
Desc
Variant0004
Relatedalso
ClinVar
Risk rs121909177(G,T;G,T)
Alt rs121909177(G,T;G,T)
Reference rs121909177(C;C)
Significance Pathogenic
Disease Thyroid dyshormonogenesis 1
Variation info
Gene SLC5A5
CLNDBN Thyroid dyshormonogenesis 1
Reversed 0
HGVS NC_000019.9:g.17999206C>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000008106.2,