rs1060499791

Orientation

plus

Stabilized

plus

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

Make rs1060499791(C;T)

Make rs1060499791(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

10

Position

71617295

Gene

CDH23

is a	snp
is	mentioned by
dbSNP	rs1060499791
dbSNP (classic)	rs1060499791
ClinGen	rs1060499791
ebi	rs1060499791
HLI	rs1060499791
Exac	rs1060499791
Gnomad	rs1060499791
Varsome	rs1060499791
LitVar	rs1060499791
Map	rs1060499791
PheGenI	rs1060499791
Biobank	rs1060499791
1000 genomes	rs1060499791
hgdp	rs1060499791
ensembl	rs1060499791
geneview	rs1060499791
scholar	rs1060499791
google	rs1060499791
pharmgkb	rs1060499791
gwascentral	rs1060499791
openSNP	rs1060499791
23andMe	rs1060499791
SNPshot	rs1060499791
SNPdbe	rs1060499791
MSV3d	rs1060499791
GWAS Ctlg	rs1060499791

Max Magnitude

0

ClinVar
Risk	rs1060499791(T;T)
Alt	rs1060499791(T;T)
Reference	Rs1060499791(C;C)
Significance	Pathogenic
Disease	Deafness
Variation	info
Gene	CDH23
CLNDBN	Deafness, autosomal recessive 12
Reversed	0
HGVS	NC_000010.10:g.73377052C>T
CLNSRC
CLNACC	RCV000454253.1,