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rs121908361

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs121908361(A;G)
Make rs121908361(G;G)
ReferenceGRCh38 38.1/141
Chromosome7
Position107689156
GeneSLC26A4
is asnp
is mentioned by
dbSNPrs121908361
ebirs121908361
HLIrs121908361
Exacrs121908361
Varsomers121908361
Maprs121908361
PheGenIrs121908361
hapmaprs121908361
1000 genomesrs121908361
hgdprs121908361
ensemblrs121908361
gopubmedrs121908361
geneviewrs121908361
scholarrs121908361
googlers121908361
pharmgkbrs121908361
gwascentralrs121908361
openSNPrs121908361
23andMers121908361
23andMe allrs121908361
SNP Nexus

SNPshotrs121908361
SNPdbers121908361
MSV3drs121908361
GWAS Ctlgrs121908361
Max Magnitude0
OMIM605646
Desc
Variant0010
Relatedalso
ClinVar
Risk rs121908361(G;G)
Alt rs121908361(G;G)
Reference rs121908361(A;A)
Significance Pathogenic
Disease Enlarged vestibular aqueduct syndrome
Variation info
Gene SLC26A4
CLNDBN Enlarged vestibular aqueduct syndrome
Reversed 0
HGVS NC_000007.13:g.107329601A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000005091.3,