rs367928692

Orientation

plus

Stabilized

plus

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

Make rs367928692(A;A)

Make rs367928692(A;G)

Reference

GRCh38 38.1/141

Chromosome

10

Position

71791123

Gene	CDH23, MIR7152

is a	snp
is	mentioned by
dbSNP	rs367928692
dbSNP (classic)	rs367928692
ClinGen	rs367928692
ebi	rs367928692
HLI	rs367928692
Exac	rs367928692
Gnomad	rs367928692
Varsome	rs367928692
LitVar	rs367928692
Map	rs367928692
PheGenI	rs367928692
Biobank	rs367928692
1000 genomes	rs367928692
hgdp	rs367928692
ensembl	rs367928692
geneview	rs367928692
scholar	rs367928692
google	rs367928692
pharmgkb	rs367928692
gwascentral	rs367928692
openSNP	rs367928692
23andMe	rs367928692
SNPshot	rs367928692
SNPdbe	rs367928692
MSV3d	rs367928692
GWAS Ctlg	rs367928692

Max Magnitude

0

ClinVar
Risk	rs367928692(A;A)
Alt	rs367928692(A;A)
Reference	Rs367928692(G;G)
Significance	Pathogenic
Disease	Usher syndrome not provided
Variation	info
Gene	MIR7152 CDH23
CLNDBN	Usher syndrome, type 1D not provided
Reversed	0
HGVS	NC_000010.10:g.73550880G>A
CLNSRC	ClinVar
CLNACC	RCV000039236.3, RCV000239237.2,