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rs387906865

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(AC;AC) 0 common in clinvar
(CA;CA) 0 common in clinvar
Make rs387906865(-;-)
Make rs387906865(-;CA)
ReferenceGRCh38 38.1/141
Chromosome4
Position106328144
GeneAIMP1
is asnp
is mentioned by
dbSNPrs387906865
ebirs387906865
HLIrs387906865
Exacrs387906865
Varsomers387906865
Maprs387906865
PheGenIrs387906865
hapmaprs387906865
1000 genomesrs387906865
hgdprs387906865
ensemblrs387906865
gopubmedrs387906865
geneviewrs387906865
scholarrs387906865
googlers387906865
pharmgkbrs387906865
gwascentralrs387906865
openSNPrs387906865
23andMers387906865
23andMe allrs387906865
SNP Nexus

SNPshotrs387906865
SNPdbers387906865
MSV3drs387906865
GWAS Ctlgrs387906865
Max Magnitude0
ClinVar
Risk rs387906865(;)
Alt rs387906865(;)
Reference rs387906865(AC;AC)
Significance Pathogenic
Disease Leukodystrophy
Variation info
Gene AIMP1
CLNDBN Leukodystrophy, hypomyelinating 3
Reversed 0
HGVS NC_000004.11:g.107249301_107249302delCA
CLNSRC OMIM Allelic Variant
CLNACC RCV000023320.3,