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rs797044558

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs797044558(A;A)
Make rs797044558(A;G)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position75053585
GeneABCB7
is asnp
is mentioned by
dbSNPrs797044558
ebirs797044558
HLIrs797044558
Exacrs797044558
Varsomers797044558
Maprs797044558
PheGenIrs797044558
hapmaprs797044558
1000 genomesrs797044558
hgdprs797044558
ensemblrs797044558
gopubmedrs797044558
geneviewrs797044558
scholarrs797044558
googlers797044558
pharmgkbrs797044558
gwascentralrs797044558
openSNPrs797044558
23andMers797044558
23andMe allrs797044558
SNP Nexus

SNPshotrs797044558
SNPdbers797044558
MSV3drs797044558
GWAS Ctlgrs797044558
Max Magnitude0
ClinVar
Risk rs797044558(A;A)
Alt rs797044558(A;A)
Reference rs797044558(G;G)
Significance Pathogenic
Disease Spinocerebellar ataxia
Variation info
Gene ABCB7
CLNDBN Spinocerebellar ataxia, X-linked
Reversed 1
HGVS NC_000023.10:g.74273420C>T
CLNSRC
CLNACC RCV000190539.1,