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rs387906581

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs387906581(-;-)
Make rs387906581(-;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position33024543
GeneAK2
is asnp
is mentioned by
dbSNPrs387906581
ebirs387906581
HLIrs387906581
Exacrs387906581
Varsomers387906581
Maprs387906581
PheGenIrs387906581
hapmaprs387906581
1000 genomesrs387906581
hgdprs387906581
ensemblrs387906581
gopubmedrs387906581
geneviewrs387906581
scholarrs387906581
googlers387906581
pharmgkbrs387906581
gwascentralrs387906581
openSNPrs387906581
23andMers387906581
23andMe allrs387906581
SNP Nexus

SNPshotrs387906581
SNPdbers387906581
MSV3drs387906581
GWAS Ctlgrs387906581
Max Magnitude0
ClinVar
Risk rs387906581(;)
Alt rs387906581(;)
Reference rs387906581(T;T)
Significance Pathogenic
Disease Reticular dysgenesis
Variation info
Gene AK2
CLNDBN Reticular dysgenesis
Reversed 1
HGVS NC_000001.10:g.33490144delA
CLNSRC OMIM Allelic Variant
CLNACC RCV000019913.27,