rs267606725

Orientation

plus

Stabilized

plus

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

Make rs267606725(C;T)

Make rs267606725(T;T)

Reference

GRCh38 38.1/141

Chromosome

2

Position

232539760

Gene

CHRNG

is a	snp
is	mentioned by
dbSNP	rs267606725
dbSNP (classic)	rs267606725
ClinGen	rs267606725
ebi	rs267606725
HLI	rs267606725
Exac	rs267606725
Gnomad	rs267606725
Varsome	rs267606725
LitVar	rs267606725
Map	rs267606725
PheGenI	rs267606725
Biobank	rs267606725
1000 genomes	rs267606725
hgdp	rs267606725
ensembl	rs267606725
geneview	rs267606725
scholar	rs267606725
google	rs267606725
pharmgkb	rs267606725
gwascentral	rs267606725
openSNP	rs267606725
23andMe	rs267606725
SNPshot	rs267606725
SNPdbe	rs267606725
MSV3d	rs267606725
GWAS Ctlg	rs267606725

Max Magnitude

0

ClinVar
Risk	rs267606725(T;T)
Alt	rs267606725(T;T)
Reference	Rs267606725(C;C)
Significance	Pathogenic
Disease	Multiple pterygium syndrome Escobar type
Variation	info
Gene	CHRNG
CLNDBN	Multiple pterygium syndrome Escobar type
Reversed	0
HGVS	NC_000002.11:g.233404470C>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000020002.27,