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rs1057516636

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057516636(-;-)
Make rs1057516636(-;C)
ReferenceGRCh38.p7 38.3/150
Chromosome7
Position107701989
GeneSLC26A4
is asnp
is mentioned by
dbSNPrs1057516636
dbSNP (old)rs1057516636
ClinGenrs1057516636
ebirs1057516636
HLIrs1057516636
Exacrs1057516636
Gnomadrs1057516636
Varsomers1057516636
LitVarrs1057516636
Maprs1057516636
PheGenIrs1057516636
Biobankrs1057516636
1000 genomesrs1057516636
hgdprs1057516636
ensemblrs1057516636
gopubmedrs1057516636
geneviewrs1057516636
scholarrs1057516636
googlers1057516636
pharmgkbrs1057516636
gwascentralrs1057516636
openSNPrs1057516636
23andMers1057516636
23andMe allrs1057516636
SNPshotrs1057516636
SNPdbers1057516636
MSV3drs1057516636
GWAS Ctlgrs1057516636
Max Magnitude0
ClinVar
Risk rs1057516636(-;-)
Alt rs1057516636(-;-)
Reference Rs1057516636(C;C)
Significance Probable-Pathogenic
Disease Pendred's syndrome
Variation info
Gene SLC26A4
CLNDBN Pendred's syndrome
Reversed 0
HGVS NC_000007.13:g.107342434delC
CLNSRC
CLNACC RCV000412428.1,