rs797044490

Orientation

plus

Stabilized

plus

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

Make rs797044490(-;-)

Make rs797044490(-;ATCC)

Make rs797044490(ATCC;ATCC)

Reference

GRCh38.p2 38.2/146

Chromosome

11

Position

77158400

Gene

MYO7A

is a	snp
is	mentioned by
dbSNP	rs797044490
dbSNP (classic)	rs797044490
ClinGen	rs797044490
ebi	rs797044490
HLI	rs797044490
Exac	rs797044490
Gnomad	rs797044490
Varsome	rs797044490
LitVar	rs797044490
Map	rs797044490
PheGenI	rs797044490
Biobank	rs797044490
1000 genomes	rs797044490
hgdp	rs797044490
ensembl	rs797044490
geneview	rs797044490
scholar	rs797044490
google	rs797044490
pharmgkb	rs797044490
gwascentral	rs797044490
openSNP	rs797044490
23andMe	rs797044490
SNPshot	rs797044490
SNPdbe	rs797044490
MSV3d	rs797044490
GWAS Ctlg	rs797044490

Max Magnitude

0

ClinVar
Risk	rs797044490(-;-)
Alt	rs797044490(-;-)
Reference	Rs797044490(CCAT;CCAT)
Significance	Pathogenic
Disease	Usher syndrome
Variation	info
Gene	MYO7A
CLNDBN	Usher syndrome, type 1
Reversed	0
HGVS	NC_000011.9:g.76869446_76869449delATCC
CLNSRC
CLNACC	RCV000151481.1,