rs876657711

Merged into

rs797044564

Orientation

plus

Stabilized

plus

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

Make rs876657711(-;-)

Make rs876657711(-;CT)

Make rs876657711(CT;CT)

Reference

GRCh38.p2 38.2/147

Chromosome

11

Position

77189431

Gene

MYO7A

is a	snp
is	mentioned by
dbSNP	rs876657711
dbSNP (classic)	rs876657711
ClinGen	rs876657711
ebi	rs876657711
HLI	rs876657711
Exac	rs876657711
Gnomad	rs876657711
Varsome	rs876657711
LitVar	rs876657711
Map	rs876657711
PheGenI	rs876657711
Biobank	rs876657711
1000 genomes	rs876657711
hgdp	rs876657711
ensembl	rs876657711
geneview	rs876657711
scholar	rs876657711
google	rs876657711
pharmgkb	rs876657711
gwascentral	rs876657711
openSNP	rs876657711
23andMe	rs876657711
SNPshot	rs876657711
SNPdbe	rs876657711
MSV3d	rs876657711
GWAS Ctlg	rs876657711

Status

Merged into rs797044564

Max Magnitude

0

ClinVar
Risk
Alt
Reference	Rs876657711(TC;TC)
Significance	Pathogenic
Disease	not provided Usher syndrome
Variation	info
Gene	MYO7A
CLNDBN	not provided Usher syndrome, type 1
Reversed	0
HGVS	NC_000011.9:g.76900476_76900477delCT
CLNSRC
CLNACC	RCV000171464.1, RCV000222358.1,