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rs886041955

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(-;-) 0 common in clinvar
Chromosome15
Position23645672
GeneMAGEL2
is asnp
is mentioned by
dbSNPrs886041955
dbSNP (classic)rs886041955
ClinGenrs886041955
ebirs886041955
HLIrs886041955
Exacrs886041955
Gnomadrs886041955
Varsomers886041955
LitVarrs886041955
Maprs886041955
PheGenIrs886041955
Biobankrs886041955
1000 genomesrs886041955
hgdprs886041955
ensemblrs886041955
geneviewrs886041955
scholarrs886041955
googlers886041955
pharmgkbrs886041955
gwascentralrs886041955
openSNPrs886041955
23andMers886041955
SNPshotrs886041955
SNPdbers886041955
MSV3drs886041955
GWAS Ctlgrs886041955
Max Magnitude0
ClinVar
Risk rs886041955(T;T)
Alt rs886041955(T;T)
Reference Rs886041955(-;-)
Significance Pathogenic
Disease not provided
Variation info
Gene MAGEL2
CLNDBN not provided
Reversed 1
HGVS NC_000015.9:g.23890820dupA
CLNSRC
CLNACC RCV000404304.1,