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rs786204730

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs786204730(-;-)
Make rs786204730(-;T)
Make rs786204730(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome7
Position107672198
GeneSLC26A4
is asnp
is mentioned by
dbSNPrs786204730
ebirs786204730
HLIrs786204730
Exacrs786204730
Varsomers786204730
Maprs786204730
PheGenIrs786204730
hapmaprs786204730
1000 genomesrs786204730
hgdprs786204730
ensemblrs786204730
gopubmedrs786204730
geneviewrs786204730
scholarrs786204730
googlers786204730
pharmgkbrs786204730
gwascentralrs786204730
openSNPrs786204730
23andMers786204730
23andMe allrs786204730
SNP Nexus

SNPshotrs786204730
SNPdbers786204730
MSV3drs786204730
GWAS Ctlgrs786204730
Max Magnitude0
ClinVar
Risk rs786204730(T;T)
Alt rs786204730(T;T)
Reference rs786204730(;)
Significance Probable-Pathogenic
Disease Pendred's syndrome
Variation info
Gene SLC26A4
CLNDBN Pendred's syndrome
Reversed 0
HGVS NC_000007.13:g.107312643dupT
CLNSRC
CLNACC RCV000169571.1,