rs876657416

Orientation

plus

Stabilized

plus

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

Make rs876657416(C;C)

Make rs876657416(C;T)

Reference

GRCh38.p2 38.2/147

Chromosome

11

Position

77174772

Gene

MYO7A

is a	snp
is	mentioned by
dbSNP	rs876657416
dbSNP (classic)	rs876657416
ClinGen	rs876657416
ebi	rs876657416
HLI	rs876657416
Exac	rs876657416
Gnomad	rs876657416
Varsome	rs876657416
LitVar	rs876657416
Map	rs876657416
PheGenI	rs876657416
Biobank	rs876657416
1000 genomes	rs876657416
hgdp	rs876657416
ensembl	rs876657416
geneview	rs876657416
scholar	rs876657416
google	rs876657416
pharmgkb	rs876657416
gwascentral	rs876657416
openSNP	rs876657416
23andMe	rs876657416
SNPshot	rs876657416
SNPdbe	rs876657416
MSV3d	rs876657416
GWAS Ctlg	rs876657416

Max Magnitude

0

ClinVar
Risk	rs876657416(C;C)
Alt	rs876657416(C;C)
Reference	Rs876657416(T;T)
Significance	Pathogenic
Disease	Usher syndrome
Variation	info
Gene	MYO7A
CLNDBN	Usher syndrome, type 1
Reversed	0
HGVS	NC_000011.9:g.76885818T>C
CLNSRC
CLNACC	RCV000219432.1,