rs397516316

Orientation

plus

Stabilized

plus

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

Make rs397516316(A;G)

Make rs397516316(G;G)

Reference

GRCh38.p2 38.2/144

Chromosome

11

Position

77204065

Gene

MYO7A

is a	snp
is	mentioned by
dbSNP	rs397516316
dbSNP (classic)	rs397516316
ClinGen	rs397516316
ebi	rs397516316
HLI	rs397516316
Exac	rs397516316
Gnomad	rs397516316
Varsome	rs397516316
LitVar	rs397516316
Map	rs397516316
PheGenI	rs397516316
Biobank	rs397516316
1000 genomes	rs397516316
hgdp	rs397516316
ensembl	rs397516316
geneview	rs397516316
scholar	rs397516316
google	rs397516316
pharmgkb	rs397516316
gwascentral	rs397516316
openSNP	rs397516316
23andMe	rs397516316
SNPshot	rs397516316
SNPdbe	rs397516316
MSV3d	rs397516316
GWAS Ctlg	rs397516316

Max Magnitude

0

ClinVar
Risk	rs397516316(G;G)
Alt	rs397516316(G;G)
Reference	Rs397516316(A;A)
Significance	Probable-Pathogenic
Disease	Usher syndrome
Variation	info
Gene	MYO7A
CLNDBN	Usher syndrome, type 1
Reversed	0
HGVS	NC_000011.9:g.76915110A>G
CLNSRC
CLNACC	RCV000036185.2,