rs199897298

Orientation

plus

Stabilized

plus

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

Make rs199897298(G;T)

Make rs199897298(T;T)

Reference

GRCh38.p2 38.2/147

Chromosome

11

Position

77184688

Gene

MYO7A

is a	snp
is	mentioned by
dbSNP	rs199897298
dbSNP (classic)	rs199897298
ClinGen	rs199897298
ebi	rs199897298
HLI	rs199897298
Exac	rs199897298
Gnomad	rs199897298
Varsome	rs199897298
LitVar	rs199897298
Map	rs199897298
PheGenI	rs199897298
Biobank	rs199897298
1000 genomes	rs199897298
hgdp	rs199897298
ensembl	rs199897298
geneview	rs199897298
scholar	rs199897298
google	rs199897298
pharmgkb	rs199897298
gwascentral	rs199897298
openSNP	rs199897298
23andMe	rs199897298
SNPshot	rs199897298
SNPdbe	rs199897298
MSV3d	rs199897298
GWAS Ctlg	rs199897298

Max Magnitude

0

ClinVar
Risk	rs199897298(T;T)
Alt	rs199897298(T;T)
Reference	Rs199897298(G;G)
Significance	Pathogenic
Disease	Usher syndrome not provided
Variation	info
Gene	MYO7A
CLNDBN	Usher syndrome, type 1 not provided
Reversed	0
HGVS	NC_000011.9:g.76895733G>T
CLNSRC
CLNACC	RCV000036110.3, RCV000312187.1,