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rs786204523

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs786204523(-;-)
Make rs786204523(-;T)
ReferenceGRCh38.p2 38.2/146
Chromosome7
Position107710091
GeneSLC26A4
is asnp
is mentioned by
dbSNPrs786204523
ebirs786204523
HLIrs786204523
Exacrs786204523
Varsomers786204523
Maprs786204523
PheGenIrs786204523
hapmaprs786204523
1000 genomesrs786204523
hgdprs786204523
ensemblrs786204523
gopubmedrs786204523
geneviewrs786204523
scholarrs786204523
googlers786204523
pharmgkbrs786204523
gwascentralrs786204523
openSNPrs786204523
23andMers786204523
23andMe allrs786204523
SNP Nexus

SNPshotrs786204523
SNPdbers786204523
MSV3drs786204523
GWAS Ctlgrs786204523
Max Magnitude0
ClinVar
Risk rs786204523(;)
Alt rs786204523(;)
Reference rs786204523(T;T)
Significance Probable-Pathogenic
Disease Pendred's syndrome
Variation info
Gene SLC26A4
CLNDBN Pendred's syndrome
Reversed 0
HGVS NC_000007.13:g.107350536delT
CLNSRC
CLNACC RCV000169223.1,