rs1060499792

Orientation

plus

Stabilized

plus

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

Make rs1060499792(C;T)

Make rs1060499792(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

10

Position

71677616

Gene

CDH23

is a	snp
is	mentioned by
dbSNP	rs1060499792
dbSNP (classic)	rs1060499792
ClinGen	rs1060499792
ebi	rs1060499792
HLI	rs1060499792
Exac	rs1060499792
Gnomad	rs1060499792
Varsome	rs1060499792
LitVar	rs1060499792
Map	rs1060499792
PheGenI	rs1060499792
Biobank	rs1060499792
1000 genomes	rs1060499792
hgdp	rs1060499792
ensembl	rs1060499792
geneview	rs1060499792
scholar	rs1060499792
google	rs1060499792
pharmgkb	rs1060499792
gwascentral	rs1060499792
openSNP	rs1060499792
23andMe	rs1060499792
SNPshot	rs1060499792
SNPdbe	rs1060499792
MSV3d	rs1060499792
GWAS Ctlg	rs1060499792

Max Magnitude

0

ClinVar
Risk	rs1060499792(T;T)
Alt	rs1060499792(T;T)
Reference	Rs1060499792(C;C)
Significance	Pathogenic
Disease	Deafness
Variation	info
Gene	CDH23
CLNDBN	Deafness, autosomal recessive 12
Reversed	0
HGVS	NC_000010.10:g.73437373C>T
CLNSRC
CLNACC	RCV000454185.1,