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rs398123105

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs398123105(C;T)
Make rs398123105(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position153740618
GeneABCD1
is asnp
is mentioned by
dbSNPrs398123105
ebirs398123105
HLIrs398123105
Exacrs398123105
Varsomers398123105
Maprs398123105
PheGenIrs398123105
hapmaprs398123105
1000 genomesrs398123105
hgdprs398123105
ensemblrs398123105
gopubmedrs398123105
geneviewrs398123105
scholarrs398123105
googlers398123105
pharmgkbrs398123105
gwascentralrs398123105
openSNPrs398123105
23andMers398123105
23andMe allrs398123105
SNP Nexus

SNPshotrs398123105
SNPdbers398123105
MSV3drs398123105
GWAS Ctlgrs398123105
Max Magnitude0
ClinVar
Risk rs398123105(T;T)
Alt rs398123105(T;T)
Reference rs398123105(C;C)
Significance Pathogenic
Disease Adrenoleukodystrophy
Variation info
Gene ABCD1
CLNDBN Adrenoleukodystrophy
Reversed 0
HGVS NC_000023.10:g.153006072C>T
CLNSRC HGMD
CLNACC RCV000077958.4,