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rs4808708

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs4808708(A;A)
Make rs4808708(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome19
Position17890877
GeneSLC5A5
is asnp
is mentioned by
dbSNPrs4808708
dbSNP (old)rs4808708
ClinGenrs4808708
ebirs4808708
HLIrs4808708
Exacrs4808708
Gnomadrs4808708
Varsomers4808708
Maprs4808708
PheGenIrs4808708
Biobankrs4808708
1000 genomesrs4808708
hgdprs4808708
ensemblrs4808708
gopubmedrs4808708
geneviewrs4808708
scholarrs4808708
googlers4808708
pharmgkbrs4808708
gwascentralrs4808708
openSNPrs4808708
23andMers4808708
23andMe allrs4808708
SNP Nexus

SNPshotrs4808708
SNPdbers4808708
MSV3drs4808708
GWAS Ctlgrs4808708
Max Magnitude0
? (A;A) (A;G) (G;G) 28
[PMID 26160439] The potential role of the sodium symporter gene polymorphism in the development of differentiated thyroid cancer


ClinVar
Risk rs4808708(A;A)
Alt rs4808708(A;A)
Reference Rs4808708(G;G)
Significance Probable-non-pathogenic
Disease not specified Thyroid Hormonogenesis Defect
Variation info
Gene SLC5A5
CLNDBN not specified Thyroid Hormonogenesis Defect
Reversed 0
HGVS NC_000019.9:g.18001686G>A
CLNSRC
CLNACC RCV000248822.1, RCV000354638.1,