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rs797044626

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs797044626(A;G)
Make rs797044626(G;G)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position153743487
GeneABCD1
is asnp
is mentioned by
dbSNPrs797044626
ebirs797044626
HLIrs797044626
Exacrs797044626
Varsomers797044626
Maprs797044626
PheGenIrs797044626
hapmaprs797044626
1000 genomesrs797044626
hgdprs797044626
ensemblrs797044626
gopubmedrs797044626
geneviewrs797044626
scholarrs797044626
googlers797044626
pharmgkbrs797044626
gwascentralrs797044626
openSNPrs797044626
23andMers797044626
23andMe allrs797044626
SNP Nexus

SNPshotrs797044626
SNPdbers797044626
MSV3drs797044626
GWAS Ctlgrs797044626
Max Magnitude0
ClinVar
Risk rs797044626(G;G)
Alt rs797044626(G;G)
Reference rs797044626(A;A)
Significance Pathogenic
Disease Adrenoleukodystrophy
Variation info
Gene ABCD1
CLNDBN Adrenoleukodystrophy
Reversed 0
HGVS NC_000023.10:g.153008941A>G
CLNSRC
CLNACC RCV000173621.1,