rs772025588

Orientation

plus

Stabilized

plus

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

Make rs772025588(A;C)

Make rs772025588(C;C)

Reference

GRCh38.p7 38.3/149

Chromosome

10

Position

49614274

Gene

CHAT

is a	snp
is	mentioned by
dbSNP	rs772025588
dbSNP (classic)	rs772025588
ClinGen	rs772025588
ebi	rs772025588
HLI	rs772025588
Exac	rs772025588
Gnomad	rs772025588
Varsome	rs772025588
LitVar	rs772025588
Map	rs772025588
PheGenI	rs772025588
Biobank	rs772025588
1000 genomes	rs772025588
hgdp	rs772025588
ensembl	rs772025588
geneview	rs772025588
scholar	rs772025588
google	rs772025588
pharmgkb	rs772025588
gwascentral	rs772025588
openSNP	rs772025588
23andMe	rs772025588
SNPshot	rs772025588
SNPdbe	rs772025588
MSV3d	rs772025588
GWAS Ctlg	rs772025588

Max Magnitude

0

ClinVar
Risk	rs772025588(C;C) rs772025588(T;T)
Alt	rs772025588(C;C) rs772025588(T;T)
Reference	Rs772025588(A;A)
Significance	Pathogenic
Disease	Familial infantile myasthenia
Variation	info
Gene	CHAT
CLNDBN	Familial infantile myasthenia
Reversed	0
HGVS	NC_000010.10:g.50822320A>T
CLNSRC
CLNACC	RCV000303776.1,