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

rs863223905

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs863223905(A;G)
Make rs863223905(G;G)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position55015667
GeneALAS2
is asnp
is mentioned by
dbSNPrs863223905
ebirs863223905
HLIrs863223905
Exacrs863223905
Varsomers863223905
Maprs863223905
PheGenIrs863223905
hapmaprs863223905
1000 genomesrs863223905
hgdprs863223905
ensemblrs863223905
gopubmedrs863223905
geneviewrs863223905
scholarrs863223905
googlers863223905
pharmgkbrs863223905
gwascentralrs863223905
openSNPrs863223905
23andMers863223905
23andMe allrs863223905
SNP Nexus

SNPshotrs863223905
SNPdbers863223905
MSV3drs863223905
GWAS Ctlgrs863223905
Max Magnitude0
ClinVar
Risk rs863223905(G;G)
Alt rs863223905(G;G)
Reference rs863223905(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene ALAS2
CLNDBN not provided
Reversed 1
HGVS NC_000023.10:g.55042100T>C
CLNSRC
CLNACC RCV000198893.1,