rs533568822

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(G;G)	0	common in clinvar

Make rs533568822(G;T)

Make rs533568822(T;T)

Reference

GRCh38.p2 38.2/144

Chromosome

18

Position

34882130

Gene

DTNA

is a	snp
is	mentioned by
dbSNP	rs533568822
dbSNP (classic)	rs533568822
ClinGen	rs533568822
ebi	rs533568822
HLI	rs533568822
Exac	rs533568822
Gnomad	rs533568822
Varsome	rs533568822
LitVar	rs533568822
Map	rs533568822
PheGenI	rs533568822
Biobank	rs533568822
1000 genomes	rs533568822
hgdp	rs533568822
ensembl	rs533568822
geneview	rs533568822
scholar	rs533568822
google	rs533568822
pharmgkb	rs533568822
gwascentral	rs533568822
openSNP	rs533568822
23andMe	rs533568822
SNPshot	rs533568822
SNPdbe	rs533568822
MSV3d	rs533568822
GWAS Ctlg	rs533568822

Max Magnitude

0

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,