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rs786204426

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs786204426(C;C)
Make rs786204426(C;G)
ReferenceGRCh38.p2 38.2/146
Chromosome7
Position107661644
GeneSLC26A4, SLC26A4-AS1
is asnp
is mentioned by
dbSNPrs786204426
ebirs786204426
HLIrs786204426
Exacrs786204426
Varsomers786204426
Maprs786204426
PheGenIrs786204426
hapmaprs786204426
1000 genomesrs786204426
hgdprs786204426
ensemblrs786204426
gopubmedrs786204426
geneviewrs786204426
scholarrs786204426
googlers786204426
pharmgkbrs786204426
gwascentralrs786204426
openSNPrs786204426
23andMers786204426
23andMe allrs786204426
SNP Nexus

SNPshotrs786204426
SNPdbers786204426
MSV3drs786204426
GWAS Ctlgrs786204426
Max Magnitude0
ClinVar
Risk rs786204426(C;C)
Alt rs786204426(C;C)
Reference rs786204426(G;G)
Significance Probable-Pathogenic
Disease Pendred's syndrome
Variation info
Gene SLC26A4-AS1 SLC26A4
CLNDBN Pendred's syndrome
Reversed 0
HGVS NC_000007.13:g.107302089G>C
CLNSRC
CLNACC RCV000169018.1,