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rs142498437

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs142498437(A;G)
Make rs142498437(G;G)
ReferenceGRCh38.p7 38.3/150
Chromosome7
Position107690212
GeneSLC26A4
is asnp
is mentioned by
dbSNPrs142498437
dbSNP (old)rs142498437
ClinGenrs142498437
ebirs142498437
HLIrs142498437
Exacrs142498437
Gnomadrs142498437
Varsomers142498437
Maprs142498437
PheGenIrs142498437
Biobankrs142498437
1000 genomesrs142498437
hgdprs142498437
ensemblrs142498437
gopubmedrs142498437
geneviewrs142498437
scholarrs142498437
googlers142498437
pharmgkbrs142498437
gwascentralrs142498437
openSNPrs142498437
23andMers142498437
23andMe allrs142498437
SNPshotrs142498437
SNPdbers142498437
MSV3drs142498437
GWAS Ctlgrs142498437
Max Magnitude0
ClinVar
Risk rs142498437(G;G)
Alt rs142498437(G;G)
Reference Rs142498437(A;A)
Significance Probable-Pathogenic
Disease Pendred's syndrome
Variation info
Gene SLC26A4
CLNDBN Pendred's syndrome
Reversed 0
HGVS NC_000007.13:g.107330657A>G
CLNSRC
CLNACC RCV000411469.1,