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rs12327843

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs12327843(C;C)
Make rs12327843(C;T)
ReferenceGRCh38.p2 38.2/144
Chromosome19
Position17894103
GeneSLC5A5
is asnp
is mentioned by
dbSNPrs12327843
dbSNP (classic)rs12327843
ClinGenrs12327843
ebirs12327843
HLIrs12327843
Exacrs12327843
Gnomadrs12327843
Varsomers12327843
LitVarrs12327843
Maprs12327843
PheGenIrs12327843
Biobankrs12327843
1000 genomesrs12327843
hgdprs12327843
ensemblrs12327843
geneviewrs12327843
scholarrs12327843
googlers12327843
pharmgkbrs12327843
gwascentralrs12327843
openSNPrs12327843
23andMers12327843
SNPshotrs12327843
SNPdbers12327843
MSV3drs12327843
GWAS Ctlgrs12327843
Max Magnitude0
? (C;C) (C;T) (T;T) 28


[PMID 26160439] The potential role of the sodium symporter gene polymorphism in the development of differentiated thyroid cancer


ClinVar
Risk rs12327843(C;C)
Alt rs12327843(C;C)
Reference Rs12327843(T;T)
Significance Probable-non-pathogenic
Disease Thyroid Hormonogenesis Defect
Variation info
Gene SLC5A5
CLNDBN Thyroid Hormonogenesis Defect
Reversed 0
HGVS NC_000019.9:g.18004912T>C
CLNSRC
CLNACC RCV000323427.1,