Have questions? Visit https://www.reddit.com/r/SNPedia

rs786204421

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs786204421(-;-)
Make rs786204421(-;T)
ReferenceGRCh38.p2 38.2/146
Chromosome7
Position107663410
GeneSLC26A4, SLC26A4-AS1
is asnp
is mentioned by
dbSNPrs786204421
ebirs786204421
HLIrs786204421
Exacrs786204421
Varsomers786204421
Maprs786204421
PheGenIrs786204421
hapmaprs786204421
1000 genomesrs786204421
hgdprs786204421
ensemblrs786204421
gopubmedrs786204421
geneviewrs786204421
scholarrs786204421
googlers786204421
pharmgkbrs786204421
gwascentralrs786204421
openSNPrs786204421
23andMers786204421
23andMe allrs786204421
SNP Nexus

SNPshotrs786204421
SNPdbers786204421
MSV3drs786204421
GWAS Ctlgrs786204421
Max Magnitude0
ClinVar
Risk rs786204421(;)
Alt rs786204421(;)
Reference rs786204421(T;T)
Significance Probable-Pathogenic
Disease Pendred's syndrome
Variation info
Gene SLC26A4-AS1 SLC26A4
CLNDBN Pendred's syndrome
Reversed 0
HGVS NC_000007.13:g.107303855delT
CLNSRC
CLNACC RCV000169009.1,