rs876657654

Orientation

plus

Stabilized

plus

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

Make rs876657654(G;G)

Make rs876657654(G;T)

Reference

GRCh38.p2 38.2/147

Chromosome

11

Position

77155935

Gene

MYO7A

is a	snp
is	mentioned by
dbSNP	rs876657654
dbSNP (classic)	rs876657654
ClinGen	rs876657654
ebi	rs876657654
HLI	rs876657654
Exac	rs876657654
Gnomad	rs876657654
Varsome	rs876657654
LitVar	rs876657654
Map	rs876657654
PheGenI	rs876657654
Biobank	rs876657654
1000 genomes	rs876657654
hgdp	rs876657654
ensembl	rs876657654
geneview	rs876657654
scholar	rs876657654
google	rs876657654
pharmgkb	rs876657654
gwascentral	rs876657654
openSNP	rs876657654
23andMe	rs876657654
SNPshot	rs876657654
SNPdbe	rs876657654
MSV3d	rs876657654
GWAS Ctlg	rs876657654

Max Magnitude

0

ClinVar
Risk	rs876657654(G;G)
Alt	rs876657654(G;G)
Reference	Rs876657654(T;T)
Significance	Probable-Pathogenic
Disease	Usher syndrome
Variation	info
Gene	MYO7A
CLNDBN	Usher syndrome, type 1
Reversed	0
HGVS	NC_000011.9:g.76866981T>G
CLNSRC
CLNACC	RCV000219484.1,