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rs431905486

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs431905486(-;-)
Make rs431905486(-;A)
Make rs431905486(A;A)
ReferenceGRCh38 38.1/141
Chromosome7
Position107683533
GeneSLC26A4
is asnp
is mentioned by
dbSNPrs431905486
ebirs431905486
HLIrs431905486
Exacrs431905486
Varsomers431905486
Maprs431905486
PheGenIrs431905486
hapmaprs431905486
1000 genomesrs431905486
hgdprs431905486
ensemblrs431905486
gopubmedrs431905486
geneviewrs431905486
scholarrs431905486
googlers431905486
pharmgkbrs431905486
gwascentralrs431905486
openSNPrs431905486
23andMers431905486
23andMe allrs431905486
SNP Nexus

SNPshotrs431905486
SNPdbers431905486
MSV3drs431905486
GWAS Ctlgrs431905486
Max Magnitude0
ClinVar
Risk rs431905486(A;A)
Alt rs431905486(A;A)
Reference rs431905486(;)
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.107323978dupA
CLNSRC ClinVar
CLNACC RCV000083261.1,