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rs786204581

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs786204581(C;T)
Make rs786204581(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome7
Position107663366
GeneSLC26A4, SLC26A4-AS1
is asnp
is mentioned by
dbSNPrs786204581
ebirs786204581
HLIrs786204581
Exacrs786204581
Varsomers786204581
Maprs786204581
PheGenIrs786204581
hapmaprs786204581
1000 genomesrs786204581
hgdprs786204581
ensemblrs786204581
gopubmedrs786204581
geneviewrs786204581
scholarrs786204581
googlers786204581
pharmgkbrs786204581
gwascentralrs786204581
openSNPrs786204581
23andMers786204581
23andMe allrs786204581
SNP Nexus

SNPshotrs786204581
SNPdbers786204581
MSV3drs786204581
GWAS Ctlgrs786204581
Max Magnitude0
ClinVar
Risk rs786204581(T;T)
Alt rs786204581(T;T)
Reference rs786204581(C;C)
Significance Probable-Pathogenic
Disease Pendred's syndrome
Variation info
Gene SLC26A4-AS1 SLC26A4
CLNDBN Pendred's syndrome
Reversed 0
HGVS NC_000007.13:g.107303811C>T
CLNSRC
CLNACC RCV000169324.1,