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rs786204474

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs786204474(C;T)
Make rs786204474(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome7
Position107689130
GeneSLC26A4
is asnp
is mentioned by
dbSNPrs786204474
ebirs786204474
HLIrs786204474
Exacrs786204474
Varsomers786204474
Maprs786204474
PheGenIrs786204474
hapmaprs786204474
1000 genomesrs786204474
hgdprs786204474
ensemblrs786204474
gopubmedrs786204474
geneviewrs786204474
scholarrs786204474
googlers786204474
pharmgkbrs786204474
gwascentralrs786204474
openSNPrs786204474
23andMers786204474
23andMe allrs786204474
SNP Nexus

SNPshotrs786204474
SNPdbers786204474
MSV3drs786204474
GWAS Ctlgrs786204474
Max Magnitude0
ClinVar
Risk rs786204474(T;T)
Alt rs786204474(T;T)
Reference rs786204474(C;C)
Significance Probable-Pathogenic
Disease Pendred's syndrome
Variation info
Gene SLC26A4
CLNDBN Pendred's syndrome
Reversed 0
HGVS NC_000007.13:g.107329575C>T
CLNSRC
CLNACC RCV000169123.1,