Have questions? Visit https://www.reddit.com/r/SNPedia

rs398123107

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs398123107(A;A)
Make rs398123107(A;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position153743008
GeneABCD1
is asnp
is mentioned by
dbSNPrs398123107
ebirs398123107
HLIrs398123107
Exacrs398123107
Varsomers398123107
Maprs398123107
PheGenIrs398123107
hapmaprs398123107
1000 genomesrs398123107
hgdprs398123107
ensemblrs398123107
gopubmedrs398123107
geneviewrs398123107
scholarrs398123107
googlers398123107
pharmgkbrs398123107
gwascentralrs398123107
openSNPrs398123107
23andMers398123107
23andMe allrs398123107
SNP Nexus

SNPshotrs398123107
SNPdbers398123107
MSV3drs398123107
GWAS Ctlgrs398123107
Max Magnitude0
ClinVar
Risk rs398123107(A;A)
Alt rs398123107(A;A)
Reference rs398123107(G;G)
Significance Pathogenic
Disease Adrenoleukodystrophy
Variation info
Gene ABCD1
CLNDBN Adrenoleukodystrophy
Reversed 0
HGVS NC_000023.10:g.153008462G>A
CLNSRC HGMD
CLNACC RCV000077960.4,