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rs886041841

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(CAG;CAG) 0 common in clinvar
Chromosome11
Position47441668
GeneRAPSN
is asnp
is mentioned by
dbSNPrs886041841
dbSNP (classic)rs886041841
ClinGenrs886041841
ebirs886041841
HLIrs886041841
Exacrs886041841
Gnomadrs886041841
Varsomers886041841
LitVarrs886041841
Maprs886041841
PheGenIrs886041841
Biobankrs886041841
1000 genomesrs886041841
hgdprs886041841
ensemblrs886041841
geneviewrs886041841
scholarrs886041841
googlers886041841
pharmgkbrs886041841
gwascentralrs886041841
openSNPrs886041841
23andMers886041841
SNPshotrs886041841
SNPdbers886041841
MSV3drs886041841
GWAS Ctlgrs886041841
Max Magnitude0
ClinVar
Risk rs886041841(TAA;TAA)
Alt rs886041841(TAA;TAA)
Reference Rs886041841(CAG;CAG)
Significance Pathogenic
Disease not provided
Variation info
Gene RAPSN
CLNDBN not provided
Reversed 1
HGVS NC_000011.9:g.47463220_47463222delCTGinsTTA
CLNSRC
CLNACC RCV000348754.1,