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rs121909179

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121909179(A;A)
Make rs121909179(A;G)
ReferenceGRCh38 38.1/141
Chromosome19
Position17888432
GeneSLC5A5
is asnp
is mentioned by
dbSNPrs121909179
ebirs121909179
HLIrs121909179
Exacrs121909179
Varsomers121909179
Maprs121909179
PheGenIrs121909179
hapmaprs121909179
1000 genomesrs121909179
hgdprs121909179
ensemblrs121909179
gopubmedrs121909179
geneviewrs121909179
scholarrs121909179
googlers121909179
pharmgkbrs121909179
gwascentralrs121909179
openSNPrs121909179
23andMers121909179
23andMe allrs121909179
SNP Nexus

SNPshotrs121909179
SNPdbers121909179
MSV3drs121909179
GWAS Ctlgrs121909179
Max Magnitude0
OMIM601843
Desc
Variant0006
Relatedalso
ClinVar
Risk rs121909179(A;A)
Alt rs121909179(A;A)
Reference rs121909179(G;G)
Significance Pathogenic
Disease Thyroid dyshormonogenesis 1
Variation info
Gene SLC5A5
CLNDBN Thyroid dyshormonogenesis 1
Reversed 0
HGVS NC_000019.9:g.17999241G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000008108.2,