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rs786204742

From SNPedia

Merged intors752807925
Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs786204742(C;T)
Make rs786204742(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome7
Position107704382
GeneSLC26A4
is asnp
is mentioned by
dbSNPrs786204742
ebirs786204742
HLIrs786204742
Exacrs786204742
Varsomers786204742
Maprs786204742
PheGenIrs786204742
hapmaprs786204742
1000 genomesrs786204742
hgdprs786204742
ensemblrs786204742
gopubmedrs786204742
geneviewrs786204742
scholarrs786204742
googlers786204742
pharmgkbrs786204742
gwascentralrs786204742
openSNPrs786204742
23andMers786204742
23andMe allrs786204742
SNP Nexus

SNPshotrs786204742
SNPdbers786204742
MSV3drs786204742
GWAS Ctlgrs786204742
StatusMerged into rs752807925
Max Magnitude0
ClinVar
Risk rs786204742(T;T)
Alt rs786204742(T;T)
Reference rs786204742(C;C)
Significance Probable-Pathogenic
Disease Pendred's syndrome
Variation info
Gene SLC26A4
CLNDBN Pendred's syndrome
Reversed 0
HGVS NC_000007.14:g.107704382C>T
CLNSRC
CLNACC RCV000169591.1,