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rs397516427

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397516427(G;T)
Make rs397516427(T;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position107710109
GeneSLC26A4
is asnp
is mentioned by
dbSNPrs397516427
ebirs397516427
HLIrs397516427
Exacrs397516427
Varsomers397516427
Maprs397516427
PheGenIrs397516427
hapmaprs397516427
1000 genomesrs397516427
hgdprs397516427
ensemblrs397516427
gopubmedrs397516427
geneviewrs397516427
scholarrs397516427
googlers397516427
pharmgkbrs397516427
gwascentralrs397516427
openSNPrs397516427
23andMers397516427
23andMe allrs397516427
SNP Nexus

SNPshotrs397516427
SNPdbers397516427
MSV3drs397516427
GWAS Ctlgrs397516427
Max Magnitude0
ClinVar
Risk rs397516427(T;T)
Alt rs397516427(T;T)
Reference rs397516427(G;G)
Significance Probable-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.107350554G>T
CLNSRC ClinVar
CLNACC RCV000036476.2,