rs763721044

Orientation

plus

Stabilized

plus

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

Make rs763721044(G;T)

Make rs763721044(T;T)

Reference

GRCh38.p2 38.2/147

Chromosome

10

Position

71805836

Gene

CDH23

is a	snp
is	mentioned by
dbSNP	rs763721044
dbSNP (classic)	rs763721044
ClinGen	rs763721044
ebi	rs763721044
HLI	rs763721044
Exac	rs763721044
Gnomad	rs763721044
Varsome	rs763721044
LitVar	rs763721044
Map	rs763721044
PheGenI	rs763721044
Biobank	rs763721044
1000 genomes	rs763721044
hgdp	rs763721044
ensembl	rs763721044
geneview	rs763721044
scholar	rs763721044
google	rs763721044
pharmgkb	rs763721044
gwascentral	rs763721044
openSNP	rs763721044
23andMe	rs763721044
SNPshot	rs763721044
SNPdbe	rs763721044
MSV3d	rs763721044
GWAS Ctlg	rs763721044

Max Magnitude

0

ClinVar
Risk	rs763721044(T;T)
Alt	rs763721044(T;T)
Reference	Rs763721044(G;G)
Significance	Pathogenic
Disease	not specified Deafness
Variation	info
Gene	CDH23
CLNDBN	not specified Deafness, autosomal recessive 12
Reversed	0
HGVS	NC_000010.10:g.73565593G>T
CLNSRC
CLNACC	RCV000216327.1, RCV000225060.1,