rs397516324

Orientation

plus

Stabilized

plus

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

Make rs397516324(C;C)

Make rs397516324(C;T)

Reference

GRCh38 38.1/141

Chromosome

11

Position

77156776

Gene

MYO7A

is a	snp
is	mentioned by
dbSNP	rs397516324
dbSNP (classic)	rs397516324
ClinGen	rs397516324
ebi	rs397516324
HLI	rs397516324
Exac	rs397516324
Gnomad	rs397516324
Varsome	rs397516324
LitVar	rs397516324
Map	rs397516324
PheGenI	rs397516324
Biobank	rs397516324
1000 genomes	rs397516324
hgdp	rs397516324
ensembl	rs397516324
geneview	rs397516324
scholar	rs397516324
google	rs397516324
pharmgkb	rs397516324
gwascentral	rs397516324
openSNP	rs397516324
23andMe	rs397516324
SNPshot	rs397516324
SNPdbe	rs397516324
MSV3d	rs397516324
GWAS Ctlg	rs397516324

Max Magnitude

0

ClinVar
Risk	rs397516324(C;C)
Alt	rs397516324(C;C)
Reference	Rs397516324(T;T)
Significance	Probable-Pathogenic
Disease	Usher syndrome
Variation	info
Gene	MYO7A
CLNDBN	Usher syndrome, type 1
Reversed	0
HGVS	NC_000011.9:g.76867822T>C
CLNSRC	ClinVar
CLNACC	RCV000036211.2,