rs1060499716

Orientation

plus

Stabilized

plus

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

Make rs1060499716(A;A)

Make rs1060499716(A;G)

Reference

GRCh38.p7 38.3/150

Chromosome

11

Position

77157397

Gene

MYO7A

is a	snp
is	mentioned by
dbSNP	rs1060499716
dbSNP (classic)	rs1060499716
ClinGen	rs1060499716
ebi	rs1060499716
HLI	rs1060499716
Exac	rs1060499716
Gnomad	rs1060499716
Varsome	rs1060499716
LitVar	rs1060499716
Map	rs1060499716
PheGenI	rs1060499716
Biobank	rs1060499716
1000 genomes	rs1060499716
hgdp	rs1060499716
ensembl	rs1060499716
geneview	rs1060499716
scholar	rs1060499716
google	rs1060499716
pharmgkb	rs1060499716
gwascentral	rs1060499716
openSNP	rs1060499716
23andMe	rs1060499716
SNPshot	rs1060499716
SNPdbe	rs1060499716
MSV3d	rs1060499716
GWAS Ctlg	rs1060499716

Max Magnitude

0

ClinVar
Risk	rs1060499716(A;A)
Alt	rs1060499716(A;A)
Reference	Rs1060499716(G;G)
Significance	Probable-Pathogenic
Disease	Usher syndrome
Variation	info
Gene	MYO7A
CLNDBN	Usher syndrome, type 1
Reversed	0
HGVS	NC_000011.9:g.76868443G>A
CLNSRC
CLNACC	RCV000449574.1,