rs181611778

Orientation

plus

Stabilized

plus

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

Make rs181611778(A;A)

Make rs181611778(A;G)

Reference

GRCh38.p7 38.3/150

Chromosome

10

Position

71778252

Gene

CDH23

is a	snp
is	mentioned by
dbSNP	rs181611778
dbSNP (classic)	rs181611778
ClinGen	rs181611778
ebi	rs181611778
HLI	rs181611778
Exac	rs181611778
Gnomad	rs181611778
Varsome	rs181611778
LitVar	rs181611778
Map	rs181611778
PheGenI	rs181611778
Biobank	rs181611778
1000 genomes	rs181611778
hgdp	rs181611778
ensembl	rs181611778
geneview	rs181611778
scholar	rs181611778
google	rs181611778
pharmgkb	rs181611778
gwascentral	rs181611778
openSNP	rs181611778
23andMe	rs181611778
SNPshot	rs181611778
SNPdbe	rs181611778
MSV3d	rs181611778
GWAS Ctlg	rs181611778

Max Magnitude

0

ClinVar
Risk	rs181611778(A;A)
Alt	rs181611778(A;A)
Reference	Rs181611778(G;G)
Significance	Probable-Pathogenic
Disease	not specified not provided
Variation	info
Gene	CDH23
CLNDBN	not specified not provided
Reversed	0
HGVS	NC_000010.10:g.73538009G>A
CLNSRC
CLNACC	RCV000178447.1, RCV000479783.1,