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rs786204502

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs786204502(A;A)
Make rs786204502(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome7
Position107701942
GeneSLC26A4
is asnp
is mentioned by
dbSNPrs786204502
ebirs786204502
HLIrs786204502
Exacrs786204502
Varsomers786204502
Maprs786204502
PheGenIrs786204502
hapmaprs786204502
1000 genomesrs786204502
hgdprs786204502
ensemblrs786204502
gopubmedrs786204502
geneviewrs786204502
scholarrs786204502
googlers786204502
pharmgkbrs786204502
gwascentralrs786204502
openSNPrs786204502
23andMers786204502
23andMe allrs786204502
SNP Nexus

SNPshotrs786204502
SNPdbers786204502
MSV3drs786204502
GWAS Ctlgrs786204502
Max Magnitude0
ClinVar
Risk rs786204502(A;A)
Alt rs786204502(A;A)
Reference rs786204502(G;G)
Significance Probable-Pathogenic
Disease Pendred's syndrome
Variation info
Gene SLC26A4
CLNDBN Pendred's syndrome
Reversed 0
HGVS NC_000007.13:g.107342387G>A
CLNSRC
CLNACC RCV000169184.1,