rs786205612

Orientation

plus

Stabilized

plus

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

Make rs786205612(-;-)

Make rs786205612(-;CCG)

Reference

GRCh38.p2 38.2/146

Chromosome

10

Position

71810549

Gene

CDH23

is a	snp
is	mentioned by
dbSNP	rs786205612
dbSNP (classic)	rs786205612
ClinGen	rs786205612
ebi	rs786205612
HLI	rs786205612
Exac	rs786205612
Gnomad	rs786205612
Varsome	rs786205612
LitVar	rs786205612
Map	rs786205612
PheGenI	rs786205612
Biobank	rs786205612
1000 genomes	rs786205612
hgdp	rs786205612
ensembl	rs786205612
geneview	rs786205612
scholar	rs786205612
google	rs786205612
pharmgkb	rs786205612
gwascentral	rs786205612
openSNP	rs786205612
23andMe	rs786205612
SNPshot	rs786205612
SNPdbe	rs786205612
MSV3d	rs786205612
GWAS Ctlg	rs786205612

Max Magnitude

0

ClinVar
Risk	rs786205612(-;-)
Alt	rs786205612(-;-)
Reference	Rs786205612(CCG;CCG)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	CDH23
CLNDBN	not provided
Reversed	0
HGVS	NC_000010.10:g.73570306_73570308delCCG
CLNSRC
CLNACC	RCV000171457.1,