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rs786205549

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs786205549(A;A)
Make rs786205549(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position232539803
GeneCHRNG
is asnp
is mentioned by
dbSNPrs786205549
ebirs786205549
HLIrs786205549
Exacrs786205549
Varsomers786205549
Maprs786205549
PheGenIrs786205549
hapmaprs786205549
1000 genomesrs786205549
hgdprs786205549
ensemblrs786205549
gopubmedrs786205549
geneviewrs786205549
scholarrs786205549
googlers786205549
pharmgkbrs786205549
gwascentralrs786205549
openSNPrs786205549
23andMers786205549
23andMe allrs786205549
SNP Nexus

SNPshotrs786205549
SNPdbers786205549
MSV3drs786205549
GWAS Ctlgrs786205549
Max Magnitude0
ClinVar
Risk rs786205549(A;A)
Alt rs786205549(A;A)
Reference rs786205549(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene CHRNG
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.233404513G>A
CLNSRC
CLNACC RCV000171338.1,