rs397516320

Orientation

plus

Stabilized

plus

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

Make rs397516320(-;C)

Make rs397516320(C;C)

Reference

GRCh38 38.1/141

Chromosome

11

Position

77205562

Gene

MYO7A

is a	snp
is	mentioned by
dbSNP	rs397516320
dbSNP (classic)	rs397516320
ClinGen	rs397516320
ebi	rs397516320
HLI	rs397516320
Exac	rs397516320
Gnomad	rs397516320
Varsome	rs397516320
LitVar	rs397516320
Map	rs397516320
PheGenI	rs397516320
Biobank	rs397516320
1000 genomes	rs397516320
hgdp	rs397516320
ensembl	rs397516320
geneview	rs397516320
scholar	rs397516320
google	rs397516320
pharmgkb	rs397516320
gwascentral	rs397516320
openSNP	rs397516320
23andMe	rs397516320
SNPshot	rs397516320
SNPdbe	rs397516320
MSV3d	rs397516320
GWAS Ctlg	rs397516320

Max Magnitude

0

ClinVar
Risk	rs397516320(C;C)
Alt	rs397516320(C;C)
Reference	Rs397516320(-;-)
Significance	Pathogenic
Disease	Usher syndrome
Variation	info
Gene	MYO7A
CLNDBN	Usher syndrome, type 1
Reversed	0
HGVS	NC_000011.9:g.76916607dupC
CLNSRC	ClinVar
CLNACC	RCV000036194.2,