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rs786204739

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs786204739(G;G)
Make rs786204739(G;T)
ReferenceGRCh38.p2 38.2/146
Chromosome7
Position107698083
GeneSLC26A4
is asnp
is mentioned by
dbSNPrs786204739
ebirs786204739
HLIrs786204739
Exacrs786204739
Varsomers786204739
Maprs786204739
PheGenIrs786204739
hapmaprs786204739
1000 genomesrs786204739
hgdprs786204739
ensemblrs786204739
gopubmedrs786204739
geneviewrs786204739
scholarrs786204739
googlers786204739
pharmgkbrs786204739
gwascentralrs786204739
openSNPrs786204739
23andMers786204739
23andMe allrs786204739
SNP Nexus

SNPshotrs786204739
SNPdbers786204739
MSV3drs786204739
GWAS Ctlgrs786204739
Max Magnitude0
ClinVar
Risk rs786204739(G;G)
Alt rs786204739(G;G)
Reference rs786204739(T;T)
Significance Probable-Pathogenic
Disease Pendred's syndrome
Variation info
Gene SLC26A4
CLNDBN Pendred's syndrome
Reversed 0
HGVS NC_000007.13:g.107338528T>G
CLNSRC
CLNACC RCV000169586.1,