rs781811444

Orientation

plus

Stabilized

plus

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

Make rs781811444(C;T)

Make rs781811444(T;T)

Reference

GRCh38.p2 38.2/146

Chromosome

11

Position

77155908

Gene

MYO7A

is a	snp
is	mentioned by
dbSNP	rs781811444
dbSNP (classic)	rs781811444
ClinGen	rs781811444
ebi	rs781811444
HLI	rs781811444
Exac	rs781811444
Gnomad	rs781811444
Varsome	rs781811444
LitVar	rs781811444
Map	rs781811444
PheGenI	rs781811444
Biobank	rs781811444
1000 genomes	rs781811444
hgdp	rs781811444
ensembl	rs781811444
geneview	rs781811444
scholar	rs781811444
google	rs781811444
pharmgkb	rs781811444
gwascentral	rs781811444
openSNP	rs781811444
23andMe	rs781811444
SNPshot	rs781811444
SNPdbe	rs781811444
MSV3d	rs781811444
GWAS Ctlg	rs781811444

Max Magnitude

0

ClinVar
Risk	rs781811444(T;T)
Alt	rs781811444(T;T)
Reference	Rs781811444(C;C)
Significance	Probable-Pathogenic
Disease	Usher syndrome
Variation	info
Gene	MYO7A
CLNDBN	Usher syndrome, type 1
Reversed	0
HGVS	NC_000011.9:g.76866954C>T
CLNSRC
CLNACC	RCV000156777.1,