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rs1057517161

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1057517161(A;A)
Make rs1057517161(A;T)
ReferenceGRCh38.p7 38.3/150
Chromosome7
Position107701972
GeneSLC26A4
is asnp
is mentioned by
dbSNPrs1057517161
dbSNP (classic)rs1057517161
ClinGenrs1057517161
ebirs1057517161
HLIrs1057517161
Exacrs1057517161
Gnomadrs1057517161
Varsomers1057517161
LitVarrs1057517161
Maprs1057517161
PheGenIrs1057517161
Biobankrs1057517161
1000 genomesrs1057517161
hgdprs1057517161
ensemblrs1057517161
geneviewrs1057517161
scholarrs1057517161
googlers1057517161
pharmgkbrs1057517161
gwascentralrs1057517161
openSNPrs1057517161
23andMers1057517161
23andMe allrs1057517161
SNPshotrs1057517161
SNPdbers1057517161
MSV3drs1057517161
GWAS Ctlgrs1057517161
Max Magnitude0
ClinVar
Risk rs1057517161(A;A)
Alt rs1057517161(A;A)
Reference Rs1057517161(T;T)
Significance Probable-Pathogenic
Disease Pendred's syndrome
Variation info
Gene SLC26A4
CLNDBN Pendred's syndrome
Reversed 0
HGVS NC_000007.13:g.107342417T>A
CLNSRC
CLNACC RCV000410627.1,