rs111033388

Orientation

plus

Stabilized

plus

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

Make rs111033388(-;TGAGCAAACAGCGGGGCTCCA)

Make rs111033388(TGAGCAAACAGCGGGGCTCCA;TGAGCAAACAGCGGGGCTCCA)

Reference

GRCh38 38.1/141

Chromosome

11

Position

77214682

Gene

MYO7A

is a	snp
is	mentioned by
dbSNP	rs111033388
dbSNP (classic)	rs111033388
ClinGen	rs111033388
ebi	rs111033388
HLI	rs111033388
Exac	rs111033388
Gnomad	rs111033388
Varsome	rs111033388
LitVar	rs111033388
Map	rs111033388
PheGenI	rs111033388
Biobank	rs111033388
1000 genomes	rs111033388
hgdp	rs111033388
ensembl	rs111033388
geneview	rs111033388
scholar	rs111033388
google	rs111033388
pharmgkb	rs111033388
gwascentral	rs111033388
openSNP	rs111033388
23andMe	rs111033388
SNPshot	rs111033388
SNPdbe	rs111033388
MSV3d	rs111033388
GWAS Ctlg	rs111033388

Max Magnitude

0

ClinVar
Risk	rs111033388(CCATGAGCAAACAGCGGGGCT;CCATGAGCAAACAGCGGGGCT) rs111033388(TGAGCAAACAGCGGGGCTCCA;TGAGCAAACAGCGGGGCTCCA)
Alt	rs111033388(CCATGAGCAAACAGCGGGGCT;CCATGAGCAAACAGCGGGGCT) rs111033388(TGAGCAAACAGCGGGGCTCCA;TGAGCAAACAGCGGGGCTCCA)
Reference	Rs111033388(-;-)
Significance	Probable-Pathogenic
Disease	Usher syndrome not specified
Variation	info
Gene	MYO7A
CLNDBN	Usher syndrome, type 1 not specified
Reversed	0
HGVS	NC_000011.9:g.76925707_76925727dup21
CLNSRC
CLNACC	RCV000154448.1, RCV000270443.1,