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rs746238617

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs746238617(C;C)
Make rs746238617(C;T)
ReferenceGRCh38.p2 38.2/144
Chromosome7
Position107663437
GeneSLC26A4, SLC26A4-AS1
is asnp
is mentioned by
dbSNPrs746238617
ebirs746238617
HLIrs746238617
Exacrs746238617
Varsomers746238617
Maprs746238617
PheGenIrs746238617
hapmaprs746238617
1000 genomesrs746238617
hgdprs746238617
ensemblrs746238617
gopubmedrs746238617
geneviewrs746238617
scholarrs746238617
googlers746238617
pharmgkbrs746238617
gwascentralrs746238617
openSNPrs746238617
23andMers746238617
23andMe allrs746238617
SNP Nexus

SNPshotrs746238617
SNPdbers746238617
MSV3drs746238617
GWAS Ctlgrs746238617
Max Magnitude0
ClinVar
Risk rs746238617(C;C)
Alt rs746238617(C;C)
Reference rs746238617(T;T)
Significance Probable-Pathogenic
Disease Pendred's syndrome
Variation info
Gene SLC26A4-AS1 SLC26A4
CLNDBN Pendred's syndrome
Reversed 0
HGVS NC_000007.13:g.107303882T>C
CLNSRC
CLNACC RCV000169595.1,