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rs1057516953

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057516953(C;T)
Make rs1057516953(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome7
Position107663412
GeneSLC26A4, SLC26A4-AS1
is asnp
is mentioned by
dbSNPrs1057516953
dbSNP (old)rs1057516953
ClinGenrs1057516953
ebirs1057516953
HLIrs1057516953
Exacrs1057516953
Gnomadrs1057516953
Varsomers1057516953
Maprs1057516953
PheGenIrs1057516953
Biobankrs1057516953
1000 genomesrs1057516953
hgdprs1057516953
ensemblrs1057516953
gopubmedrs1057516953
geneviewrs1057516953
scholarrs1057516953
googlers1057516953
pharmgkbrs1057516953
gwascentralrs1057516953
openSNPrs1057516953
23andMers1057516953
23andMe allrs1057516953
SNPshotrs1057516953
SNPdbers1057516953
MSV3drs1057516953
GWAS Ctlgrs1057516953
Max Magnitude0
ClinVar
Risk rs1057516953(T;T)
Alt rs1057516953(T;T)
Reference Rs1057516953(C;C)
Significance Pathogenic
Disease Pendred's syndrome
Variation info
Gene SLC26A4-AS1 SLC26A4
CLNDBN Pendred's syndrome
Reversed 0
HGVS NC_000007.13:g.107303857C>T
CLNSRC
CLNACC RCV000411778.1,