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rs797044610

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs797044610(A;G)
Make rs797044610(G;G)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position153726153
GeneABCD1, BCAP31
is asnp
is mentioned by
dbSNPrs797044610
ebirs797044610
HLIrs797044610
Exacrs797044610
Varsomers797044610
Maprs797044610
PheGenIrs797044610
hapmaprs797044610
1000 genomesrs797044610
hgdprs797044610
ensemblrs797044610
gopubmedrs797044610
geneviewrs797044610
scholarrs797044610
googlers797044610
pharmgkbrs797044610
gwascentralrs797044610
openSNPrs797044610
23andMers797044610
23andMe allrs797044610
SNP Nexus

SNPshotrs797044610
SNPdbers797044610
MSV3drs797044610
GWAS Ctlgrs797044610
Max Magnitude0
ClinVar
Risk rs797044610(G;G)
Alt rs797044610(G;G)
Reference rs797044610(A;A)
Significance Pathogenic
Disease Adrenoleukodystrophy
Variation info
Gene BCAP31 ABCD1
CLNDBN Adrenoleukodystrophy
Reversed 0
HGVS NC_000023.10:g.152991608A>G
CLNSRC
CLNACC RCV000173051.1,