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rs1057517298

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057517298(G;T)
Make rs1057517298(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome7
Position107694620
GeneSLC26A4
is asnp
is mentioned by
dbSNPrs1057517298
dbSNP (classic)rs1057517298
ClinGenrs1057517298
ebirs1057517298
HLIrs1057517298
Exacrs1057517298
Gnomadrs1057517298
Varsomers1057517298
LitVarrs1057517298
Maprs1057517298
PheGenIrs1057517298
Biobankrs1057517298
1000 genomesrs1057517298
hgdprs1057517298
ensemblrs1057517298
geneviewrs1057517298
scholarrs1057517298
googlers1057517298
pharmgkbrs1057517298
gwascentralrs1057517298
openSNPrs1057517298
23andMers1057517298
23andMe allrs1057517298
SNPshotrs1057517298
SNPdbers1057517298
MSV3drs1057517298
GWAS Ctlgrs1057517298
Max Magnitude0
ClinVar
Risk rs1057517298(T;T)
Alt rs1057517298(T;T)
Reference Rs1057517298(G;G)
Significance Probable-Pathogenic
Disease Pendred's syndrome
Variation info
Gene SLC26A4
CLNDBN Pendred's syndrome
Reversed 0
HGVS NC_000007.13:g.107335065G>T
CLNSRC
CLNACC RCV000410038.1,