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rs1057516658

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057516658(A;A)
Make rs1057516658(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome7
Position107663380
GeneSLC26A4, SLC26A4-AS1
is asnp
is mentioned by
dbSNPrs1057516658
dbSNP (classic)rs1057516658
ClinGenrs1057516658
ebirs1057516658
HLIrs1057516658
Exacrs1057516658
Gnomadrs1057516658
Varsomers1057516658
LitVarrs1057516658
Maprs1057516658
PheGenIrs1057516658
Biobankrs1057516658
1000 genomesrs1057516658
hgdprs1057516658
ensemblrs1057516658
geneviewrs1057516658
scholarrs1057516658
googlers1057516658
pharmgkbrs1057516658
gwascentralrs1057516658
openSNPrs1057516658
23andMers1057516658
23andMe allrs1057516658
SNPshotrs1057516658
SNPdbers1057516658
MSV3drs1057516658
GWAS Ctlgrs1057516658
Max Magnitude0
ClinVar
Risk rs1057516658(A;A)
Alt rs1057516658(A;A)
Reference Rs1057516658(G;G)
Significance Pathogenic
Disease Pendred's syndrome
Variation info
Gene SLC26A4-AS1 SLC26A4
CLNDBN Pendred's syndrome
Reversed 0
HGVS NC_000007.13:g.107303825G>A
CLNSRC
CLNACC RCV000409492.1,