rs886043716

Orientation

plus

Stabilized

plus

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

Chromosome

X

Position

85963715

Gene

CHM

is a	snp
is	mentioned by
dbSNP	rs886043716
dbSNP (classic)	rs886043716
ClinGen	rs886043716
ebi	rs886043716
HLI	rs886043716
Exac	rs886043716
Gnomad	rs886043716
Varsome	rs886043716
LitVar	rs886043716
Map	rs886043716
PheGenI	rs886043716
Biobank	rs886043716
1000 genomes	rs886043716
hgdp	rs886043716
ensembl	rs886043716
geneview	rs886043716
scholar	rs886043716
google	rs886043716
pharmgkb	rs886043716
gwascentral	rs886043716
openSNP	rs886043716
23andMe	rs886043716
SNPshot	rs886043716
SNPdbe	rs886043716
MSV3d	rs886043716
GWAS Ctlg	rs886043716

Max Magnitude

0

ClinVar
Risk	rs886043716(-;-)
Alt	rs886043716(-;-)
Reference	Rs886043716(AGTA;AGTA)
Significance	Pathogenic
Disease	Choroideremia
Variation	info
Gene	CHM
CLNDBN	Choroideremia
Reversed	0
HGVS	NC_000023.10:g.85218720_85218723delAGTA
CLNSRC
CLNACC	RCV000374975.1,