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rs886041490

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Chromosome17
Position7454395
GeneCHRNB1
is asnp
is mentioned by
dbSNPrs886041490
dbSNP (classic)rs886041490
ClinGenrs886041490
ebirs886041490
HLIrs886041490
Exacrs886041490
Gnomadrs886041490
Varsomers886041490
LitVarrs886041490
Maprs886041490
PheGenIrs886041490
Biobankrs886041490
1000 genomesrs886041490
hgdprs886041490
ensemblrs886041490
geneviewrs886041490
scholarrs886041490
googlers886041490
pharmgkbrs886041490
gwascentralrs886041490
openSNPrs886041490
23andMers886041490
SNPshotrs886041490
SNPdbers886041490
MSV3drs886041490
GWAS Ctlgrs886041490
Max Magnitude0
ClinVar
Risk rs886041490(-;-)
Alt rs886041490(-;-)
Reference Rs886041490(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene CHRNB1
CLNDBN not provided
Reversed 0
HGVS NC_000017.10:g.7357714delA
CLNSRC
CLNACC RCV000338656.1,