rs1060499793

Orientation

plus

Stabilized

plus

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

Make rs1060499793(A;A)

Make rs1060499793(A;G)

Reference

GRCh38.p7 38.3/150

Chromosome

10

Position

71709172

Gene

CDH23

is a	snp
is	mentioned by
dbSNP	rs1060499793
dbSNP (classic)	rs1060499793
ClinGen	rs1060499793
ebi	rs1060499793
HLI	rs1060499793
Exac	rs1060499793
Gnomad	rs1060499793
Varsome	rs1060499793
LitVar	rs1060499793
Map	rs1060499793
PheGenI	rs1060499793
Biobank	rs1060499793
1000 genomes	rs1060499793
hgdp	rs1060499793
ensembl	rs1060499793
geneview	rs1060499793
scholar	rs1060499793
google	rs1060499793
pharmgkb	rs1060499793
gwascentral	rs1060499793
openSNP	rs1060499793
23andMe	rs1060499793
SNPshot	rs1060499793
SNPdbe	rs1060499793
MSV3d	rs1060499793
GWAS Ctlg	rs1060499793

Max Magnitude

0

ClinVar
Risk	rs1060499793(A;A)
Alt	rs1060499793(A;A)
Reference	Rs1060499793(G;G)
Significance	Pathogenic
Disease	Deafness
Variation	info
Gene	CDH23
CLNDBN	Deafness, autosomal recessive 12
Reversed	0
HGVS	NC_000010.10:g.73468929G>A
CLNSRC
CLNACC	RCV000454274.1,