rs397516317

Orientation

plus

Stabilized

plus

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

Make rs397516317(C;T)

Make rs397516317(T;T)

Reference

GRCh38 38.1/141

Chromosome

11

Position

77204141

Gene

MYO7A

is a	snp
is	mentioned by
dbSNP	rs397516317
dbSNP (classic)	rs397516317
ClinGen	rs397516317
ebi	rs397516317
HLI	rs397516317
Exac	rs397516317
Gnomad	rs397516317
Varsome	rs397516317
LitVar	rs397516317
Map	rs397516317
PheGenI	rs397516317
Biobank	rs397516317
1000 genomes	rs397516317
hgdp	rs397516317
ensembl	rs397516317
geneview	rs397516317
scholar	rs397516317
google	rs397516317
pharmgkb	rs397516317
gwascentral	rs397516317
openSNP	rs397516317
23andMe	rs397516317
SNPshot	rs397516317
SNPdbe	rs397516317
MSV3d	rs397516317
GWAS Ctlg	rs397516317

Max Magnitude

0

ClinVar
Risk	rs397516317(T;T)
Alt	rs397516317(T;T)
Reference	Rs397516317(C;C)
Significance	Pathogenic
Disease	Usher syndrome not provided
Variation	info
Gene	MYO7A
CLNDBN	Usher syndrome, type 1 not provided
Reversed	0
HGVS	NC_000011.9:g.76915186C>T
CLNSRC	ClinVar
CLNACC	RCV000036187.2, RCV000413379.1,