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rs397516428

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs397516428(C;T)
Make rs397516428(T;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position107710152
GeneSLC26A4
is asnp
is mentioned by
dbSNPrs397516428
ebirs397516428
HLIrs397516428
Exacrs397516428
Varsomers397516428
Maprs397516428
PheGenIrs397516428
hapmaprs397516428
1000 genomesrs397516428
hgdprs397516428
ensemblrs397516428
gopubmedrs397516428
geneviewrs397516428
scholarrs397516428
googlers397516428
pharmgkbrs397516428
gwascentralrs397516428
openSNPrs397516428
23andMers397516428
23andMe allrs397516428
SNP Nexus

SNPshotrs397516428
SNPdbers397516428
MSV3drs397516428
GWAS Ctlgrs397516428
Max Magnitude0
ClinVar
Risk rs397516428(T;T)
Alt rs397516428(T;T)
Reference rs397516428(C;C)
Significance Pathogenic
Disease Enlarged vestibular aqueduct syndrome Pendred's syndrome
Variation info
Gene SLC26A4
CLNDBN Enlarged vestibular aqueduct syndrome Pendred's syndrome
Reversed 0
HGVS NC_000007.13:g.107350597C>T
CLNSRC ClinVar
CLNACC RCV000036478.2,