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rs533568822

From SNPedia

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Geno Mag Summary
(G;G) 0 common in clinvar
Make rs533568822(G;T)
Make rs533568822(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome18
Position34882130
GeneDTNA
is asnp
is mentioned by
dbSNPrs533568822
ebirs533568822
HLIrs533568822
Exacrs533568822
Varsomers533568822
Maprs533568822
PheGenIrs533568822
hapmaprs533568822
1000 genomesrs533568822
hgdprs533568822
ensemblrs533568822
gopubmedrs533568822
geneviewrs533568822
scholarrs533568822
googlers533568822
pharmgkbrs533568822
gwascentralrs533568822
openSNPrs533568822
23andMers533568822
23andMe allrs533568822
SNP Nexus

SNPshotrs533568822
SNPdbers533568822
MSV3drs533568822
GWAS Ctlgrs533568822
Max Magnitude0
ClinVar
Risk rs533568822(T;T)
Alt rs533568822(T;T)
Reference rs533568822(G;G)
Significance Probable-Pathogenic
Disease Ménière's disease
Variation info
Gene DTNA
CLNDBN Ménière's disease
Reversed 0
HGVS NC_000018.9:g.32462094G>T
CLNSRC
CLNACC RCV000149520.1,