Have questions? Visit https://www.reddit.com/r/SNPedia

rs863223902

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs863223902(C;C)
Make rs863223902(C;T)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position55015653
GeneALAS2
is asnp
is mentioned by
dbSNPrs863223902
ebirs863223902
HLIrs863223902
Exacrs863223902
Varsomers863223902
Maprs863223902
PheGenIrs863223902
hapmaprs863223902
1000 genomesrs863223902
hgdprs863223902
ensemblrs863223902
gopubmedrs863223902
geneviewrs863223902
scholarrs863223902
googlers863223902
pharmgkbrs863223902
gwascentralrs863223902
openSNPrs863223902
23andMers863223902
23andMe allrs863223902
SNP Nexus

SNPshotrs863223902
SNPdbers863223902
MSV3drs863223902
GWAS Ctlgrs863223902
Max Magnitude0
ClinVar
Risk rs863223902(C;C)
Alt rs863223902(C;C)
Reference rs863223902(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene ALAS2
CLNDBN not provided
Reversed 1
HGVS NC_000023.10:g.55042086A>G
CLNSRC
CLNACC RCV000200342.1,