rs1060499788

Orientation

plus

Stabilized

plus

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

Make rs1060499788(A;T)

Make rs1060499788(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

10

Position

71570848

Gene

CDH23

is a	snp
is	mentioned by
dbSNP	rs1060499788
dbSNP (classic)	rs1060499788
ClinGen	rs1060499788
ebi	rs1060499788
HLI	rs1060499788
Exac	rs1060499788
Gnomad	rs1060499788
Varsome	rs1060499788
LitVar	rs1060499788
Map	rs1060499788
PheGenI	rs1060499788
Biobank	rs1060499788
1000 genomes	rs1060499788
hgdp	rs1060499788
ensembl	rs1060499788
geneview	rs1060499788
scholar	rs1060499788
google	rs1060499788
pharmgkb	rs1060499788
gwascentral	rs1060499788
openSNP	rs1060499788
23andMe	rs1060499788
SNPshot	rs1060499788
SNPdbe	rs1060499788
MSV3d	rs1060499788
GWAS Ctlg	rs1060499788

Max Magnitude

0

ClinVar
Risk	rs1060499788(T;T)
Alt	rs1060499788(T;T)
Reference	Rs1060499788(A;A)
Significance	Pathogenic
Disease	Deafness
Variation	info
Gene	LOC101929085 CDH23
CLNDBN	Deafness, autosomal recessive 12
Reversed	0
HGVS	NC_000010.10:g.73330605A>T
CLNSRC
CLNACC	RCV000454219.1,