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rs1060499808

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1060499808(C;C)
Make rs1060499808(C;T)
ReferenceGRCh38.p7 38.3/150
Chromosome7
Position107704344
GeneSLC26A4
is asnp
is mentioned by
dbSNPrs1060499808
dbSNP (classic)rs1060499808
ClinGenrs1060499808
ebirs1060499808
HLIrs1060499808
Exacrs1060499808
Gnomadrs1060499808
Varsomers1060499808
LitVarrs1060499808
Maprs1060499808
PheGenIrs1060499808
Biobankrs1060499808
1000 genomesrs1060499808
hgdprs1060499808
ensemblrs1060499808
geneviewrs1060499808
scholarrs1060499808
googlers1060499808
pharmgkbrs1060499808
gwascentralrs1060499808
openSNPrs1060499808
23andMers1060499808
23andMe allrs1060499808
SNPshotrs1060499808
SNPdbers1060499808
MSV3drs1060499808
GWAS Ctlgrs1060499808
Max Magnitude0
ClinVar
Risk rs1060499808(C;C)
Alt rs1060499808(C;C)
Reference Rs1060499808(T;T)
Significance Pathogenic
Disease Pendred's syndrome
Variation info
Gene SLC26A4
CLNDBN Pendred's syndrome
Reversed 0
HGVS NC_000007.13:g.107344789T>C
CLNSRC
CLNACC RCV000454307.1,