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rs797044883

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs797044883(C;T)
Make rs797044883(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome15
Position23645831
GeneMAGEL2
is asnp
is mentioned by
dbSNPrs797044883
ebirs797044883
HLIrs797044883
Exacrs797044883
Varsomers797044883
Maprs797044883
PheGenIrs797044883
hapmaprs797044883
1000 genomesrs797044883
hgdprs797044883
ensemblrs797044883
gopubmedrs797044883
geneviewrs797044883
scholarrs797044883
googlers797044883
pharmgkbrs797044883
gwascentralrs797044883
openSNPrs797044883
23andMers797044883
23andMe allrs797044883
SNP Nexus

SNPshotrs797044883
SNPdbers797044883
MSV3drs797044883
GWAS Ctlgrs797044883
Max Magnitude0
ClinVar
Risk rs797044883(T;T)
Alt rs797044883(T;T)
Reference rs797044883(C;C)
Significance Pathogenic
Disease Inborn genetic diseases not provided
Variation info
Gene MAGEL2
CLNDBN Inborn genetic diseases not provided
Reversed 1
HGVS NC_000015.9:g.23890978G>A
CLNSRC
CLNACC RCV000190699.1, RCV000238706.1,