rs111033347

Orientation

plus

Stabilized

plus

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

Make rs111033347(-;-)

Make rs111033347(-;A)

Reference

GRCh38 38.1/141

Chromosome

11

Position

77190710

Gene

MYO7A

is a	snp
is	mentioned by
dbSNP	rs111033347
dbSNP (classic)	rs111033347
ClinGen	rs111033347
ebi	rs111033347
HLI	rs111033347
Exac	rs111033347
Gnomad	rs111033347
Varsome	rs111033347
LitVar	rs111033347
Map	rs111033347
PheGenI	rs111033347
Biobank	rs111033347
1000 genomes	rs111033347
hgdp	rs111033347
ensembl	rs111033347
geneview	rs111033347
scholar	rs111033347
google	rs111033347
pharmgkb	rs111033347
gwascentral	rs111033347
openSNP	rs111033347
23andMe	rs111033347
SNPshot	rs111033347
SNPdbe	rs111033347
MSV3d	rs111033347
GWAS Ctlg	rs111033347

Max Magnitude

0

ClinVar
Risk	rs111033347(-;-)
Alt	rs111033347(-;-)
Reference	Rs111033347(A;A)
Significance	Other
Disease	Usher syndrome Deafness
Variation	info
Gene	MYO7A
CLNDBN	Usher syndrome, type 1 Deafness, autosomal recessive 2
Reversed	0
HGVS	NC_000011.9:g.76901755delA
CLNSRC	ClinVar
CLNACC	RCV000036127.2, RCV000412422.1,

[PMID 17361009] MYO7A mutation screening in Usher syndrome type I patients from diverse origins.