rs267606726

Orientation

plus

Stabilized

plus

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

Make rs267606726(G;G)

Make rs267606726(G;T)

Reference

GRCh38 38.1/141

Chromosome

2

Position

232540681

Gene

CHRNG

is a	snp
is	mentioned by
dbSNP	rs267606726
dbSNP (classic)	rs267606726
ClinGen	rs267606726
ebi	rs267606726
HLI	rs267606726
Exac	rs267606726
Gnomad	rs267606726
Varsome	rs267606726
LitVar	rs267606726
Map	rs267606726
PheGenI	rs267606726
Biobank	rs267606726
1000 genomes	rs267606726
hgdp	rs267606726
ensembl	rs267606726
geneview	rs267606726
scholar	rs267606726
google	rs267606726
pharmgkb	rs267606726
gwascentral	rs267606726
openSNP	rs267606726
23andMe	rs267606726
SNPshot	rs267606726
SNPdbe	rs267606726
MSV3d	rs267606726
GWAS Ctlg	rs267606726

Max Magnitude

0

ClinVar
Risk	rs267606726(G;G)
Alt	rs267606726(G;G)
Reference	Rs267606726(T;T)
Significance	Pathogenic
Disease	Multiple pterygium syndrome Escobar type Lethal multiple pterygium syndrome
Variation	info
Gene	CHRNG
CLNDBN	Multiple pterygium syndrome Escobar type Lethal multiple pterygium syndrome
Reversed	0
HGVS	NC_000002.11:g.233405391T>G
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000020007.29, RCV000020008.29,