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rs864309520

From SNPedia

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Geno Mag Summary
(G;G) 0 common in clinvar
Make rs864309520(C;C)
Make rs864309520(C;G)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position153725917
GeneABCD1, BCAP31
is asnp
is mentioned by
dbSNPrs864309520
ebirs864309520
HLIrs864309520
Exacrs864309520
Varsomers864309520
Maprs864309520
PheGenIrs864309520
hapmaprs864309520
1000 genomesrs864309520
hgdprs864309520
ensemblrs864309520
gopubmedrs864309520
geneviewrs864309520
scholarrs864309520
googlers864309520
pharmgkbrs864309520
gwascentralrs864309520
openSNPrs864309520
23andMers864309520
23andMe allrs864309520
SNP Nexus

SNPshotrs864309520
SNPdbers864309520
MSV3drs864309520
GWAS Ctlgrs864309520
Max Magnitude0
ClinVar
Risk rs864309520(C;C)
Alt rs864309520(C;C)
Reference rs864309520(G;G)
Significance Probable-Pathogenic
Disease Adrenoleukodystrophy
Variation info
Gene BCAP31 ABCD1
CLNDBN Adrenoleukodystrophy
Reversed 0
HGVS NC_000023.10:g.152991372G>C
CLNSRC
CLNACC RCV000202647.1,