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

rs797044781

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs797044781(A;A)
Make rs797044781(A;G)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position153742986
GeneABCD1
is asnp
is mentioned by
dbSNPrs797044781
ebirs797044781
HLIrs797044781
Exacrs797044781
Varsomers797044781
Maprs797044781
PheGenIrs797044781
hapmaprs797044781
1000 genomesrs797044781
hgdprs797044781
ensemblrs797044781
gopubmedrs797044781
geneviewrs797044781
scholarrs797044781
googlers797044781
pharmgkbrs797044781
gwascentralrs797044781
openSNPrs797044781
23andMers797044781
23andMe allrs797044781
SNP Nexus

SNPshotrs797044781
SNPdbers797044781
MSV3drs797044781
GWAS Ctlgrs797044781
Max Magnitude0
ClinVar
Risk rs797044781(A;A)
Alt rs797044781(A;A)
Reference rs797044781(G;G)
Significance Pathogenic
Disease Adrenoleukodystrophy
Variation info
Gene ABCD1
CLNDBN Adrenoleukodystrophy
Reversed 0
HGVS NC_000023.10:g.153008440G>A
CLNSRC
CLNACC RCV000180095.1,