rs797044677

Orientation

plus

Stabilized

plus

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

Make rs797044677(-;C)

Make rs797044677(C;C)

Reference

GRCh38.p2 38.2/146

Chromosome

2

Position

232540053

Gene

CHRNG

is a	snp
is	mentioned by
dbSNP	rs797044677
dbSNP (classic)	rs797044677
ClinGen	rs797044677
ebi	rs797044677
HLI	rs797044677
Exac	rs797044677
Gnomad	rs797044677
Varsome	rs797044677
LitVar	rs797044677
Map	rs797044677
PheGenI	rs797044677
Biobank	rs797044677
1000 genomes	rs797044677
hgdp	rs797044677
ensembl	rs797044677
geneview	rs797044677
scholar	rs797044677
google	rs797044677
pharmgkb	rs797044677
gwascentral	rs797044677
openSNP	rs797044677
23andMe	rs797044677
SNPshot	rs797044677
SNPdbe	rs797044677
MSV3d	rs797044677
GWAS Ctlg	rs797044677

Max Magnitude

0

ClinVar
Risk	rs797044677(C;C)
Alt	rs797044677(C;C)
Reference	Rs797044677(-;-)
Significance	Pathogenic
Disease	Multiple pterygium syndrome Escobar type not provided
Variation	info
Gene	CHRNG
CLNDBN	Multiple pterygium syndrome Escobar type not provided
Reversed	0
HGVS	NC_000002.11:g.233404763dupC
CLNSRC
CLNACC	RCV000175799.1, RCV000374812.1,