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rs886044777

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 7.7 X-linked adrenoleukodystrophy; symptoms and age of onset highly variable
(A;G) 4.4 Carrier of of X-linked adrenoleukodystrophy mutation; AMN symptoms possible
(G;G) 0 common in clinvar
ChromosomeX
Position153736196
GeneABCD1
is asnp
is mentioned by
dbSNPrs886044777
dbSNP (classic)rs886044777
ClinGenrs886044777
ebirs886044777
HLIrs886044777
Exacrs886044777
Gnomadrs886044777
Varsomers886044777
LitVarrs886044777
Maprs886044777
PheGenIrs886044777
Biobankrs886044777
1000 genomesrs886044777
hgdprs886044777
ensemblrs886044777
geneviewrs886044777
scholarrs886044777
googlers886044777
pharmgkbrs886044777
gwascentralrs886044777
openSNPrs886044777
23andMers886044777
SNPshotrs886044777
SNPdbers886044777
MSV3drs886044777
GWAS Ctlgrs886044777
Max Magnitude7.7
ClinVar
Risk Rs886044777(A;A)
Alt Rs886044777(A;A)
Reference Rs886044777(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene ABCD1
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.153001650G>A
CLNSRC
CLNACC RCV000268436.1,