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rs863223903

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs863223903(C;C)
Make rs863223903(C;T)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position55015610
GeneALAS2
is asnp
is mentioned by
dbSNPrs863223903
ebirs863223903
HLIrs863223903
Exacrs863223903
Varsomers863223903
Maprs863223903
PheGenIrs863223903
hapmaprs863223903
1000 genomesrs863223903
hgdprs863223903
ensemblrs863223903
gopubmedrs863223903
geneviewrs863223903
scholarrs863223903
googlers863223903
pharmgkbrs863223903
gwascentralrs863223903
openSNPrs863223903
23andMers863223903
23andMe allrs863223903
SNP Nexus

SNPshotrs863223903
SNPdbers863223903
MSV3drs863223903
GWAS Ctlgrs863223903
Max Magnitude0
ClinVar
Risk rs863223903(C;C)
Alt rs863223903(C;C)
Reference rs863223903(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene ALAS2
CLNDBN not provided
Reversed 1
HGVS NC_000023.10:g.55042043A>G
CLNSRC
CLNACC RCV000197406.1,