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rs1057516678

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057516678(C;T)
Make rs1057516678(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome7
Position107674963
GeneSLC26A4
is asnp
is mentioned by
dbSNPrs1057516678
dbSNP (old)rs1057516678
ClinGenrs1057516678
ebirs1057516678
HLIrs1057516678
Exacrs1057516678
Gnomadrs1057516678
Varsomers1057516678
Maprs1057516678
PheGenIrs1057516678
Biobankrs1057516678
1000 genomesrs1057516678
hgdprs1057516678
ensemblrs1057516678
gopubmedrs1057516678
geneviewrs1057516678
scholarrs1057516678
googlers1057516678
pharmgkbrs1057516678
gwascentralrs1057516678
openSNPrs1057516678
23andMers1057516678
23andMe allrs1057516678
SNPshotrs1057516678
SNPdbers1057516678
MSV3drs1057516678
GWAS Ctlgrs1057516678
Max Magnitude0
ClinVar
Risk rs1057516678(T;T)
Alt rs1057516678(T;T)
Reference Rs1057516678(C;C)
Significance Probable-Pathogenic
Disease Pendred's syndrome
Variation info
Gene SLC26A4
CLNDBN Pendred's syndrome
Reversed 0
HGVS NC_000007.13:g.107315408C>T
CLNSRC
CLNACC RCV000411641.1,