rs747067203

Orientation

plus

Stabilized

plus

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

Make rs747067203(-;-)

Make rs747067203(-;CT)

Reference

GRCh38.p7 38.3/150

Chromosome

2

Position

232541424

Gene

CHRNG

is a	snp
is	mentioned by
dbSNP	rs747067203
dbSNP (classic)	rs747067203
ClinGen	rs747067203
ebi	rs747067203
HLI	rs747067203
Exac	rs747067203
Gnomad	rs747067203
Varsome	rs747067203
LitVar	rs747067203
Map	rs747067203
PheGenI	rs747067203
Biobank	rs747067203
1000 genomes	rs747067203
hgdp	rs747067203
ensembl	rs747067203
geneview	rs747067203
scholar	rs747067203
google	rs747067203
pharmgkb	rs747067203
gwascentral	rs747067203
openSNP	rs747067203
23andMe	rs747067203
SNPshot	rs747067203
SNPdbe	rs747067203
MSV3d	rs747067203
GWAS Ctlg	rs747067203

Max Magnitude

0

ClinVar
Risk	rs747067203(-;-)
Alt	rs747067203(-;-)
Reference	Rs747067203(CT;CT)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	CHRNG
CLNDBN	not provided
Reversed	0
HGVS	NC_000002.11:g.233406134_233406135delCT
CLNSRC
CLNACC	RCV000486079.1,