rs727503329

Orientation

plus

Stabilized

plus

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

Make rs727503329(A;A)

Make rs727503329(A;G)

Reference

GRCh38.p2 38.2/144

Chromosome

11

Position

77190838

Gene

MYO7A

is a	snp
is	mentioned by
dbSNP	rs727503329
dbSNP (classic)	rs727503329
ClinGen	rs727503329
ebi	rs727503329
HLI	rs727503329
Exac	rs727503329
Gnomad	rs727503329
Varsome	rs727503329
LitVar	rs727503329
Map	rs727503329
PheGenI	rs727503329
Biobank	rs727503329
1000 genomes	rs727503329
hgdp	rs727503329
ensembl	rs727503329
geneview	rs727503329
scholar	rs727503329
google	rs727503329
pharmgkb	rs727503329
gwascentral	rs727503329
openSNP	rs727503329
23andMe	rs727503329
SNPshot	rs727503329
SNPdbe	rs727503329
MSV3d	rs727503329
GWAS Ctlg	rs727503329

Max Magnitude

0

ClinVar
Risk	rs727503329(A;A)
Alt	rs727503329(A;A)
Reference	Rs727503329(G;G)
Significance	Probable-Pathogenic
Disease	Usher syndrome
Variation	info
Gene	MYO7A
CLNDBN	Usher syndrome, type 1
Reversed	0
HGVS	NC_000011.9:g.76901883G>A
CLNSRC
CLNACC	RCV000151505.2,