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rs786204601

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs786204601(-;-)
Make rs786204601(-;T)
ReferenceGRCh38.p2 38.2/146
Chromosome7
Position107696015
GeneSLC26A4
is asnp
is mentioned by
dbSNPrs786204601
ebirs786204601
HLIrs786204601
Exacrs786204601
Varsomers786204601
Maprs786204601
PheGenIrs786204601
hapmaprs786204601
1000 genomesrs786204601
hgdprs786204601
ensemblrs786204601
gopubmedrs786204601
geneviewrs786204601
scholarrs786204601
googlers786204601
pharmgkbrs786204601
gwascentralrs786204601
openSNPrs786204601
23andMers786204601
23andMe allrs786204601
SNP Nexus

SNPshotrs786204601
SNPdbers786204601
MSV3drs786204601
GWAS Ctlgrs786204601
Max Magnitude0
ClinVar
Risk rs786204601(;)
Alt rs786204601(;)
Reference rs786204601(T;T)
Significance Probable-Pathogenic
Disease Pendred's syndrome
Variation info
Gene SLC26A4
CLNDBN Pendred's syndrome
Reversed 0
HGVS NC_000007.13:g.107336460delT
CLNSRC
CLNACC RCV000169357.1,