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rs863223901

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs863223901(A;A)
Make rs863223901(A;G)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position55021084
GeneALAS2
is asnp
is mentioned by
dbSNPrs863223901
ebirs863223901
HLIrs863223901
Exacrs863223901
Varsomers863223901
Maprs863223901
PheGenIrs863223901
hapmaprs863223901
1000 genomesrs863223901
hgdprs863223901
ensemblrs863223901
gopubmedrs863223901
geneviewrs863223901
scholarrs863223901
googlers863223901
pharmgkbrs863223901
gwascentralrs863223901
openSNPrs863223901
23andMers863223901
23andMe allrs863223901
SNP Nexus

SNPshotrs863223901
SNPdbers863223901
MSV3drs863223901
GWAS Ctlgrs863223901
Max Magnitude0
ClinVar
Risk rs863223901(A;A)
Alt rs863223901(A;A)
Reference rs863223901(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene ALAS2
CLNDBN not provided
Reversed 1
HGVS NC_000023.10:g.55047517C>T
CLNSRC
CLNACC RCV000198449.1,