rs1060499790

Orientation

plus

Stabilized

plus

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

Make rs1060499790(C;C)

Make rs1060499790(C;T)

Reference

GRCh38.p7 38.3/150

Chromosome

10

Position

71807302

Gene

CDH23

is a	snp
is	mentioned by
dbSNP	rs1060499790
dbSNP (classic)	rs1060499790
ClinGen	rs1060499790
ebi	rs1060499790
HLI	rs1060499790
Exac	rs1060499790
Gnomad	rs1060499790
Varsome	rs1060499790
LitVar	rs1060499790
Map	rs1060499790
PheGenI	rs1060499790
Biobank	rs1060499790
1000 genomes	rs1060499790
hgdp	rs1060499790
ensembl	rs1060499790
geneview	rs1060499790
scholar	rs1060499790
google	rs1060499790
pharmgkb	rs1060499790
gwascentral	rs1060499790
openSNP	rs1060499790
23andMe	rs1060499790
SNPshot	rs1060499790
SNPdbe	rs1060499790
MSV3d	rs1060499790
GWAS Ctlg	rs1060499790

Max Magnitude

0

ClinVar
Risk	rs1060499790(C;C)
Alt	rs1060499790(C;C)
Reference	Rs1060499790(T;T)
Significance	Pathogenic
Disease	Deafness
Variation	info
Gene	CDH23
CLNDBN	Deafness, autosomal recessive 12
Reversed	0
HGVS	NC_000010.10:g.73567059T>C
CLNSRC
CLNACC	RCV000454163.1,