rs786205549

Orientation

plus

Stabilized

plus

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

Make rs786205549(A;A)

Make rs786205549(A;G)

Reference

GRCh38.p2 38.2/146

Chromosome

2

Position

232539803

Gene

CHRNG

is a	snp
is	mentioned by
dbSNP	rs786205549
dbSNP (classic)	rs786205549
ClinGen	rs786205549
ebi	rs786205549
HLI	rs786205549
Exac	rs786205549
Gnomad	rs786205549
Varsome	rs786205549
LitVar	rs786205549
Map	rs786205549
PheGenI	rs786205549
Biobank	rs786205549
1000 genomes	rs786205549
hgdp	rs786205549
ensembl	rs786205549
geneview	rs786205549
scholar	rs786205549
google	rs786205549
pharmgkb	rs786205549
gwascentral	rs786205549
openSNP	rs786205549
23andMe	rs786205549
SNPshot	rs786205549
SNPdbe	rs786205549
MSV3d	rs786205549
GWAS Ctlg	rs786205549

Max Magnitude

0

ClinVar
Risk	rs786205549(A;A)
Alt	rs786205549(A;A)
Reference	Rs786205549(G;G)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	CHRNG
CLNDBN	not provided
Reversed	0
HGVS	NC_000002.11:g.233404513G>A
CLNSRC
CLNACC	RCV000171338.1,