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rs797044677

From SNPedia

Orientationplus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs797044677(-;C)
Make rs797044677(C;C)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position232540053
GeneCHRNG
is asnp
is mentioned by
dbSNPrs797044677
ClinGenrs797044677
ebirs797044677
HLIrs797044677
Exacrs797044677
Varsomers797044677
Maprs797044677
PheGenIrs797044677
hapmaprs797044677
1000 genomesrs797044677
hgdprs797044677
ensemblrs797044677
gopubmedrs797044677
geneviewrs797044677
scholarrs797044677
googlers797044677
pharmgkbrs797044677
gwascentralrs797044677
openSNPrs797044677
23andMers797044677
23andMe allrs797044677
SNP Nexus

SNPshotrs797044677
SNPdbers797044677
MSV3drs797044677
GWAS Ctlgrs797044677
Max Magnitude0
ClinVar
Risk rs797044677(C;C)
Alt rs797044677(C;C)
Reference Rs797044677(;)
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.233404763dupC
CLNSRC
CLNACC RCV000175799.1,