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rs200455203

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs200455203(C;C)
Make rs200455203(C;G)
ReferenceGRCh38.p2 38.2/144
Chromosome7
Position107701998
GeneSLC26A4
is asnp
is mentioned by
dbSNPrs200455203
ebirs200455203
HLIrs200455203
Exacrs200455203
Varsomers200455203
Maprs200455203
PheGenIrs200455203
hapmaprs200455203
1000 genomesrs200455203
hgdprs200455203
ensemblrs200455203
gopubmedrs200455203
geneviewrs200455203
scholarrs200455203
googlers200455203
pharmgkbrs200455203
gwascentralrs200455203
openSNPrs200455203
23andMers200455203
23andMe allrs200455203
SNP Nexus

SNPshotrs200455203
SNPdbers200455203
MSV3drs200455203
GWAS Ctlgrs200455203
Max Magnitude0
ClinVar
Risk rs200455203(C;C)
Alt rs200455203(C;C)
Reference rs200455203(G;G)
Significance Probable-Pathogenic
Disease Pendred's syndrome
Variation info
Gene SLC26A4
CLNDBN Pendred's syndrome
Reversed 0
HGVS NC_000007.13:g.107342443G>C
CLNSRC
CLNACC RCV000169245.1,