rs527236085

Orientation

plus

Stabilized

plus

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

Make rs527236085(G;T)

Make rs527236085(T;T)

Reference

GRCh38 38.1/142

Chromosome

11

Position

77162965

Gene

MYO7A

is a	snp
is	mentioned by
dbSNP	rs527236085
dbSNP (classic)	rs527236085
ClinGen	rs527236085
ebi	rs527236085
HLI	rs527236085
Exac	rs527236085
Gnomad	rs527236085
Varsome	rs527236085
LitVar	rs527236085
Map	rs527236085
PheGenI	rs527236085
Biobank	rs527236085
1000 genomes	rs527236085
hgdp	rs527236085
ensembl	rs527236085
geneview	rs527236085
scholar	rs527236085
google	rs527236085
pharmgkb	rs527236085
gwascentral	rs527236085
openSNP	rs527236085
23andMe	rs527236085
SNPshot	rs527236085
SNPdbe	rs527236085
MSV3d	rs527236085
GWAS Ctlg	rs527236085

Max Magnitude

0

ClinVar
Risk	rs527236085(T;T)
Alt	rs527236085(T;T)
Reference	Rs527236085(G;G)
Significance	Probable-Pathogenic
Disease	Retinitis pigmentosa
Variation	info
Gene	MYO7A
CLNDBN	Retinitis pigmentosa
Reversed	0
HGVS	NC_000011.9:g.76874011G>T
CLNSRC	ClinVar
CLNACC	RCV000132570.1,