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rs786204458

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs786204458(A;G)
Make rs786204458(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome7
Position107663294
GeneSLC26A4, SLC26A4-AS1
is asnp
is mentioned by
dbSNPrs786204458
ebirs786204458
HLIrs786204458
Exacrs786204458
Varsomers786204458
Maprs786204458
PheGenIrs786204458
hapmaprs786204458
1000 genomesrs786204458
hgdprs786204458
ensemblrs786204458
gopubmedrs786204458
geneviewrs786204458
scholarrs786204458
googlers786204458
pharmgkbrs786204458
gwascentralrs786204458
openSNPrs786204458
23andMers786204458
23andMe allrs786204458
SNP Nexus

SNPshotrs786204458
SNPdbers786204458
MSV3drs786204458
GWAS Ctlgrs786204458
Max Magnitude0
ClinVar
Risk rs786204458(G;G)
Alt rs786204458(G;G)
Reference rs786204458(A;A)
Significance Probable-Pathogenic
Disease Pendred's syndrome
Variation info
Gene SLC26A4-AS1 SLC26A4
CLNDBN Pendred's syndrome
Reversed 0
HGVS NC_000007.13:g.107303739A>G
CLNSRC
CLNACC RCV000169098.1,