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rs786204504

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs786204504(-;-)
Make rs786204504(-;G)
ReferenceGRCh38.p2 38.2/146
Chromosome7
Position107661806
GeneSLC26A4, SLC26A4-AS1
is asnp
is mentioned by
dbSNPrs786204504
ebirs786204504
HLIrs786204504
Exacrs786204504
Varsomers786204504
Maprs786204504
PheGenIrs786204504
hapmaprs786204504
1000 genomesrs786204504
hgdprs786204504
ensemblrs786204504
gopubmedrs786204504
geneviewrs786204504
scholarrs786204504
googlers786204504
pharmgkbrs786204504
gwascentralrs786204504
openSNPrs786204504
23andMers786204504
23andMe allrs786204504
SNP Nexus

SNPshotrs786204504
SNPdbers786204504
MSV3drs786204504
GWAS Ctlgrs786204504
Max Magnitude0
ClinVar
Risk rs786204504(;)
Alt rs786204504(;)
Reference rs786204504(G;G)
Significance Probable-Pathogenic
Disease Pendred's syndrome
Variation info
Gene SLC26A4-AS1 SLC26A4
CLNDBN Pendred's syndrome
Reversed 0
HGVS NC_000007.13:g.107302251delG
CLNSRC
CLNACC RCV000169187.1,