rs397517329

Orientation

plus

Stabilized

plus

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

Make rs397517329(C;T)

Make rs397517329(T;T)

Reference

GRCh38 38.1/141

Chromosome

10

Position

71738597

Gene	CDH23, C10orf105

is a	snp
is	mentioned by
dbSNP	rs397517329
dbSNP (classic)	rs397517329
ClinGen	rs397517329
ebi	rs397517329
HLI	rs397517329
Exac	rs397517329
Gnomad	rs397517329
Varsome	rs397517329
LitVar	rs397517329
Map	rs397517329
PheGenI	rs397517329
Biobank	rs397517329
1000 genomes	rs397517329
hgdp	rs397517329
ensembl	rs397517329
geneview	rs397517329
scholar	rs397517329
google	rs397517329
pharmgkb	rs397517329
gwascentral	rs397517329
openSNP	rs397517329
23andMe	rs397517329
SNPshot	rs397517329
SNPdbe	rs397517329
MSV3d	rs397517329
GWAS Ctlg	rs397517329

Max Magnitude

0

ClinVar
Risk	rs397517329(T;T)
Alt	rs397517329(T;T)
Reference	Rs397517329(C;C)
Significance	Pathogenic
Disease	Usher syndrome not provided
Variation	info
Gene	C10orf105 CDH23
CLNDBN	Usher syndrome, type 1D not provided
Reversed	0
HGVS	NC_000010.10:g.73498354C>T
CLNSRC	ClinVar
CLNACC	RCV000039177.3, RCV000438508.1,