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rs145073701

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 7.7 X-linked adrenoleukodystrophy; symptoms and age of onset highly variable
(A;C) 4.4 Carrier of of X-linked adrenoleukodystrophy mutation; AMN symptoms possible
(C;C) 0 common/normal
Make rs145073701(C;T)
Make rs145073701(T;T)
ReferenceGRCh38.p7 38.3/150
ChromosomeX
Position153740184
GeneABCD1
is asnp
is mentioned by
dbSNPrs145073701
dbSNP (classic)rs145073701
ClinGenrs145073701
ebirs145073701
HLIrs145073701
Exacrs145073701
Gnomadrs145073701
Varsomers145073701
LitVarrs145073701
Maprs145073701
PheGenIrs145073701
Biobankrs145073701
1000 genomesrs145073701
hgdprs145073701
ensemblrs145073701
geneviewrs145073701
scholarrs145073701
googlers145073701
pharmgkbrs145073701
gwascentralrs145073701
openSNPrs145073701
23andMers145073701
SNPshotrs145073701
SNPdbers145073701
MSV3drs145073701
GWAS Ctlgrs145073701
Max Magnitude7.7