rs1057519500

Orientation

plus

Stabilized

plus

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

Make rs1057519500(A;A)

Make rs1057519500(A;G)

Reference

GRCh38.p7 38.3/150

Chromosome

10

Position

71566790

Gene

CDH23

is a	snp
is	mentioned by
dbSNP	rs1057519500
dbSNP (classic)	rs1057519500
ClinGen	rs1057519500
ebi	rs1057519500
HLI	rs1057519500
Exac	rs1057519500
Gnomad	rs1057519500
Varsome	rs1057519500
LitVar	rs1057519500
Map	rs1057519500
PheGenI	rs1057519500
Biobank	rs1057519500
1000 genomes	rs1057519500
hgdp	rs1057519500
ensembl	rs1057519500
geneview	rs1057519500
scholar	rs1057519500
google	rs1057519500
pharmgkb	rs1057519500
gwascentral	rs1057519500
openSNP	rs1057519500
23andMe	rs1057519500
SNPshot	rs1057519500
SNPdbe	rs1057519500
MSV3d	rs1057519500
GWAS Ctlg	rs1057519500

Max Magnitude

0

ClinVar
Risk	rs1057519500(A;A)
Alt	rs1057519500(A;A)
Reference	Rs1057519500(G;G)
Significance	Probable-Pathogenic
Disease	Deafness
Variation	info
Gene	LOC101929085 CDH23
CLNDBN	Deafness, autosomal recessive 12
Reversed	0
HGVS	NC_000010.10:g.73326547G>A
CLNSRC
CLNACC	RCV000416554.1,