rs878853378

Orientation

plus

Stabilized

plus

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

Make rs878853378(A;A)

Make rs878853378(A;C)

Reference

GRCh38.p2 38.2/147

Chromosome

11

Position

77174796

Gene

MYO7A

is a	snp
is	mentioned by
dbSNP	rs878853378
dbSNP (classic)	rs878853378
ClinGen	rs878853378
ebi	rs878853378
HLI	rs878853378
Exac	rs878853378
Gnomad	rs878853378
Varsome	rs878853378
LitVar	rs878853378
Map	rs878853378
PheGenI	rs878853378
Biobank	rs878853378
1000 genomes	rs878853378
hgdp	rs878853378
ensembl	rs878853378
geneview	rs878853378
scholar	rs878853378
google	rs878853378
pharmgkb	rs878853378
gwascentral	rs878853378
openSNP	rs878853378
23andMe	rs878853378
SNPshot	rs878853378
SNPdbe	rs878853378
MSV3d	rs878853378
GWAS Ctlg	rs878853378

Max Magnitude

0

ClinVar
Risk	rs878853378(A;A)
Alt	rs878853378(A;A)
Reference	Rs878853378(C;C)
Significance	Probable-Pathogenic
Disease	Retinal dystrophy
Variation	info
Gene	MYO7A
CLNDBN	Retinal dystrophy
Reversed	0
HGVS	NC_000011.9:g.76885842C>A
CLNSRC
CLNACC	RCV000225435.1,