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rs121908360

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs121908360(G;G)
Make rs121908360(G;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position107702023
GeneSLC26A4
is asnp
is mentioned by
dbSNPrs121908360
ebirs121908360
HLIrs121908360
Exacrs121908360
Varsomers121908360
Maprs121908360
PheGenIrs121908360
hapmaprs121908360
1000 genomesrs121908360
hgdprs121908360
ensemblrs121908360
gopubmedrs121908360
geneviewrs121908360
scholarrs121908360
googlers121908360
pharmgkbrs121908360
gwascentralrs121908360
openSNPrs121908360
23andMers121908360
23andMe allrs121908360
SNP Nexus

SNPshotrs121908360
SNPdbers121908360
MSV3drs121908360
GWAS Ctlgrs121908360
Max Magnitude0
OMIM605646
Desc
Variant0001
Relatedalso
ClinVar
Risk rs121908360(G;G)
Alt rs121908360(G;G)
Reference rs121908360(T;T)
Significance Pathogenic
Disease Pendred's syndrome
Variation info
Gene SLC26A4
CLNDBN Pendred's syndrome
Reversed 0
HGVS NC_000007.13:g.107342468T>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000005081.3,