Have questions? Visit https://www.reddit.com/r/SNPedia

rs1057516634

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1057516634(-;-)
Make rs1057516634(-;A)
ReferenceGRCh38.p7 38.3/150
Chromosome7
Position107661696
GeneSLC26A4, SLC26A4-AS1
is asnp
is mentioned by
dbSNPrs1057516634
dbSNP (old)rs1057516634
ClinGenrs1057516634
ebirs1057516634
HLIrs1057516634
Exacrs1057516634
Gnomadrs1057516634
Varsomers1057516634
Maprs1057516634
PheGenIrs1057516634
Biobankrs1057516634
1000 genomesrs1057516634
hgdprs1057516634
ensemblrs1057516634
gopubmedrs1057516634
geneviewrs1057516634
scholarrs1057516634
googlers1057516634
pharmgkbrs1057516634
gwascentralrs1057516634
openSNPrs1057516634
23andMers1057516634
23andMe allrs1057516634
SNPshotrs1057516634
SNPdbers1057516634
MSV3drs1057516634
GWAS Ctlgrs1057516634
Max Magnitude0
ClinVar
Risk rs1057516634(-;-)
Alt rs1057516634(-;-)
Reference Rs1057516634(A;A)
Significance Probable-Pathogenic
Disease Pendred's syndrome
Variation info
Gene SLC26A4-AS1 SLC26A4
CLNDBN Pendred's syndrome
Reversed 0
HGVS NC_000007.13:g.107302141delA
CLNSRC
CLNACC RCV000410259.1,