rs797044564

Orientation

plus

Stabilized

plus

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

Make rs797044564(-;-)

Make rs797044564(-;TC)

Reference

GRCh38.p2 38.2/146

Chromosome

11

Position

77189426

Gene

MYO7A

is a	snp
is	mentioned by
dbSNP	rs797044564
dbSNP (classic)	rs797044564
ClinGen	rs797044564
ebi	rs797044564
HLI	rs797044564
Exac	rs797044564
Gnomad	rs797044564
Varsome	rs797044564
LitVar	rs797044564
Map	rs797044564
PheGenI	rs797044564
Biobank	rs797044564
1000 genomes	rs797044564
hgdp	rs797044564
ensembl	rs797044564
geneview	rs797044564
scholar	rs797044564
google	rs797044564
pharmgkb	rs797044564
gwascentral	rs797044564
openSNP	rs797044564
23andMe	rs797044564
SNPshot	rs797044564
SNPdbe	rs797044564
MSV3d	rs797044564
GWAS Ctlg	rs797044564

Merged from

Rs876657711

Max Magnitude

0

ClinVar
Risk	rs797044564(-;-) rs797044564(CT;CT)
Alt	rs797044564(-;-) rs797044564(CT;CT)
Reference	Rs797044564(TC;TC)
Significance	Pathogenic
Disease	not provided Usher syndrome
Variation	info
Gene	MYO7A
CLNDBN	not provided Usher syndrome, type 1
Reversed	0
HGVS	NC_000011.9:g.76900476_76900477delCT
CLNSRC
CLNACC	RCV000171464.1, RCV000222358.1,