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rs267606725

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs267606725(C;T)
Make rs267606725(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position232539760
GeneCHRNG
is asnp
is mentioned by
dbSNPrs267606725
ebirs267606725
HLIrs267606725
Exacrs267606725
Varsomers267606725
Maprs267606725
PheGenIrs267606725
hapmaprs267606725
1000 genomesrs267606725
hgdprs267606725
ensemblrs267606725
gopubmedrs267606725
geneviewrs267606725
scholarrs267606725
googlers267606725
pharmgkbrs267606725
gwascentralrs267606725
openSNPrs267606725
23andMers267606725
23andMe allrs267606725
SNP Nexus

SNPshotrs267606725
SNPdbers267606725
MSV3drs267606725
GWAS Ctlgrs267606725
Max Magnitude0
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,