rs201479289

Orientation

plus

Stabilized

plus

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

Make rs201479289(A;A)

Make rs201479289(A;G)

Reference

GRCh38.p7 38.3/149

Chromosome

10

Position

49619743

Gene

CHAT

is a	snp
is	mentioned by
dbSNP	rs201479289
dbSNP (classic)	rs201479289
ClinGen	rs201479289
ebi	rs201479289
HLI	rs201479289
Exac	rs201479289
Gnomad	rs201479289
Varsome	rs201479289
LitVar	rs201479289
Map	rs201479289
PheGenI	rs201479289
Biobank	rs201479289
1000 genomes	rs201479289
hgdp	rs201479289
ensembl	rs201479289
geneview	rs201479289
scholar	rs201479289
google	rs201479289
pharmgkb	rs201479289
gwascentral	rs201479289
openSNP	rs201479289
23andMe	rs201479289
SNPshot	rs201479289
SNPdbe	rs201479289
MSV3d	rs201479289
GWAS Ctlg	rs201479289

Max Magnitude

0

ClinVar
Risk	rs201479289(A;A)
Alt	rs201479289(A;A)
Reference	Rs201479289(G;G)
Significance	Pathogenic
Disease	not specified not provided
Variation	info
Gene	CHAT
CLNDBN	not specified not provided
Reversed	0
HGVS	NC_000010.10:g.50827789G>A
CLNSRC
CLNACC	RCV000260686.1, RCV000331340.1,