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rs111033200

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs111033200(C;G)
Make rs111033200(G;G)
ReferenceGRCh38 38.1/141
Chromosome7
Position107663301
GeneSLC26A4
is asnp
is mentioned by
dbSNPrs111033200
ebirs111033200
HLIrs111033200
Exacrs111033200
Varsomers111033200
Maprs111033200
PheGenIrs111033200
hapmaprs111033200
1000 genomesrs111033200
hgdprs111033200
ensemblrs111033200
gopubmedrs111033200
geneviewrs111033200
scholarrs111033200
googlers111033200
pharmgkbrs111033200
gwascentralrs111033200
openSNPrs111033200
23andMers111033200
23andMe allrs111033200
SNP Nexus

SNPshotrs111033200
SNPdbers111033200
MSV3drs111033200
GWAS Ctlgrs111033200
Max Magnitude0
ClinVar
Risk rs111033200(A,G;A,G)
Alt rs111033200(A,G;A,G)
Reference rs111033200(C;C)
Significance Probable-Pathogenic
Disease Enlarged vestibular aqueduct syndrome Pendred's syndrome
Variation info
Gene SLC26A4-AS1 SLC26A4
CLNDBN Enlarged vestibular aqueduct syndrome Pendred's syndrome
Reversed 0
HGVS NC_000007.13:g.107303746C>G
CLNSRC ClinVar
CLNACC RCV000036457.2,