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rs797044611

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs797044611(C;C)
Make rs797044611(C;T)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position153726152
GeneABCD1, BCAP31
is asnp
is mentioned by
dbSNPrs797044611
ebirs797044611
HLIrs797044611
Exacrs797044611
Varsomers797044611
Maprs797044611
PheGenIrs797044611
hapmaprs797044611
1000 genomesrs797044611
hgdprs797044611
ensemblrs797044611
gopubmedrs797044611
geneviewrs797044611
scholarrs797044611
googlers797044611
pharmgkbrs797044611
gwascentralrs797044611
openSNPrs797044611
23andMers797044611
23andMe allrs797044611
SNP Nexus

SNPshotrs797044611
SNPdbers797044611
MSV3drs797044611
GWAS Ctlgrs797044611
Max Magnitude0
ClinVar
Risk rs797044611(C;C)
Alt rs797044611(C;C)
Reference rs797044611(T;T)
Significance Probable-Pathogenic
Disease Adrenoleukodystrophy
Variation info
Gene BCAP31 ABCD1
CLNDBN Adrenoleukodystrophy
Reversed 0
HGVS NC_000023.10:g.152991607T>C
CLNSRC
CLNACC RCV000173053.1,