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

rs1057516881

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1057516881(A;A)
Make rs1057516881(A;T)
ReferenceGRCh38.p7 38.3/150
Chromosome7
Position107674350
GeneSLC26A4
is asnp
is mentioned by
dbSNPrs1057516881
dbSNP (old)rs1057516881
ClinGenrs1057516881
ebirs1057516881
HLIrs1057516881
Exacrs1057516881
Gnomadrs1057516881
Varsomers1057516881
Maprs1057516881
PheGenIrs1057516881
Biobankrs1057516881
1000 genomesrs1057516881
hgdprs1057516881
ensemblrs1057516881
gopubmedrs1057516881
geneviewrs1057516881
scholarrs1057516881
googlers1057516881
pharmgkbrs1057516881
gwascentralrs1057516881
openSNPrs1057516881
23andMers1057516881
23andMe allrs1057516881
SNPshotrs1057516881
SNPdbers1057516881
MSV3drs1057516881
GWAS Ctlgrs1057516881
Max Magnitude0
ClinVar
Risk rs1057516881(A;A)
Alt rs1057516881(A;A)
Reference Rs1057516881(T;T)
Significance Pathogenic
Disease Pendred's syndrome
Variation info
Gene SLC26A4
CLNDBN Pendred's syndrome
Reversed 0
HGVS NC_000007.13:g.107314795T>A
CLNSRC
CLNACC RCV000412454.1,