rs776256380

Orientation

plus

Stabilized

plus

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

Make rs776256380(A;A)

Make rs776256380(A;G)

Reference

GRCh38.p7 38.3/149

Chromosome

X

Position

85958965

Gene

CHM

is a	snp
is	mentioned by
dbSNP	rs776256380
dbSNP (classic)	rs776256380
ClinGen	rs776256380
ebi	rs776256380
HLI	rs776256380
Exac	rs776256380
Gnomad	rs776256380
Varsome	rs776256380
LitVar	rs776256380
Map	rs776256380
PheGenI	rs776256380
Biobank	rs776256380
1000 genomes	rs776256380
hgdp	rs776256380
ensembl	rs776256380
geneview	rs776256380
scholar	rs776256380
google	rs776256380
pharmgkb	rs776256380
gwascentral	rs776256380
openSNP	rs776256380
23andMe	rs776256380
SNPshot	rs776256380
SNPdbe	rs776256380
MSV3d	rs776256380
GWAS Ctlg	rs776256380

Max Magnitude

0

ClinVar
Risk	rs776256380(A;A)
Alt	rs776256380(A;A)
Reference	Rs776256380(G;G)
Significance	Pathogenic
Disease	Choroideremia
Variation	info
Gene	CHM
CLNDBN	Choroideremia
Reversed	0
HGVS	NC_000023.10:g.85213970G>A
CLNSRC
CLNACC	RCV000302207.1,