rs111033201

Orientation

plus

Stabilized

plus

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

Make rs111033201(C;T)

Make rs111033201(T;T)

Reference

GRCh38 38.1/141

Chromosome

11

Position

77174825

Gene

MYO7A

is a	snp
is	mentioned by
dbSNP	rs111033201
dbSNP (classic)	rs111033201
ClinGen	rs111033201
ebi	rs111033201
HLI	rs111033201
Exac	rs111033201
Gnomad	rs111033201
Varsome	rs111033201
LitVar	rs111033201
Map	rs111033201
PheGenI	rs111033201
Biobank	rs111033201
1000 genomes	rs111033201
hgdp	rs111033201
ensembl	rs111033201
geneview	rs111033201
scholar	rs111033201
google	rs111033201
pharmgkb	rs111033201
gwascentral	rs111033201
openSNP	rs111033201
23andMe	rs111033201
SNPshot	rs111033201
SNPdbe	rs111033201
MSV3d	rs111033201
GWAS Ctlg	rs111033201

Max Magnitude

0

ClinVar
Risk	rs111033201(A;A) rs111033201(G;G) rs111033201(T;T)
Alt	rs111033201(A;A) rs111033201(G;G) rs111033201(T;T)
Reference	Rs111033201(C;C)
Significance	Other
Disease	Usher syndrome Deafness not provided
Variation	info
Gene	MYO7A
CLNDBN	Usher syndrome, type 1 Deafness, autosomal recessive 2 not provided
Reversed	0
HGVS	NC_000011.9:g.76885871C>T
CLNSRC	ClinVar
CLNACC	RCV000036073.2, RCV000409801.1, RCV000443077.1,

[PMID 9718356] Mutations in the myosin VIIA gene cause a wide phenotypic spectrum, including atypical Usher syndrome.