rs1060499789

Orientation

plus

Stabilized

plus

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

Make rs1060499789(A;A)

Make rs1060499789(A;G)

Reference

GRCh38.p7 38.3/150

Chromosome

10

Position

71785667

Gene

CDH23

is a	snp
is	mentioned by
dbSNP	rs1060499789
dbSNP (classic)	rs1060499789
ClinGen	rs1060499789
ebi	rs1060499789
HLI	rs1060499789
Exac	rs1060499789
Gnomad	rs1060499789
Varsome	rs1060499789
LitVar	rs1060499789
Map	rs1060499789
PheGenI	rs1060499789
Biobank	rs1060499789
1000 genomes	rs1060499789
hgdp	rs1060499789
ensembl	rs1060499789
geneview	rs1060499789
scholar	rs1060499789
google	rs1060499789
pharmgkb	rs1060499789
gwascentral	rs1060499789
openSNP	rs1060499789
23andMe	rs1060499789
SNPshot	rs1060499789
SNPdbe	rs1060499789
MSV3d	rs1060499789
GWAS Ctlg	rs1060499789

Max Magnitude

0

ClinVar
Risk	rs1060499789(A;A)
Alt	rs1060499789(A;A)
Reference	Rs1060499789(G;G)
Significance	Pathogenic
Disease	Deafness
Variation	info
Gene	CDH23
CLNDBN	Deafness, autosomal recessive 12
Reversed	0
HGVS	NC_000010.10:g.73545424G>A
CLNSRC
CLNACC	RCV000454137.1,