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rs863223904

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs863223904(A;A)
Make rs863223904(A;G)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position55014829
GeneALAS2
is asnp
is mentioned by
dbSNPrs863223904
ebirs863223904
HLIrs863223904
Exacrs863223904
Varsomers863223904
Maprs863223904
PheGenIrs863223904
hapmaprs863223904
1000 genomesrs863223904
hgdprs863223904
ensemblrs863223904
gopubmedrs863223904
geneviewrs863223904
scholarrs863223904
googlers863223904
pharmgkbrs863223904
gwascentralrs863223904
openSNPrs863223904
23andMers863223904
23andMe allrs863223904
SNP Nexus

SNPshotrs863223904
SNPdbers863223904
MSV3drs863223904
GWAS Ctlgrs863223904
Max Magnitude0
ClinVar
Risk rs863223904(A;A)
Alt rs863223904(A;A)
Reference rs863223904(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene ALAS2
CLNDBN not provided
Reversed 1
HGVS NC_000023.10:g.55041262C>T
CLNSRC
CLNACC RCV000200462.1,