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rs863223906

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs863223906(A;G)
Make rs863223906(G;G)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position55009245
GeneALAS2
is asnp
is mentioned by
dbSNPrs863223906
ebirs863223906
HLIrs863223906
Exacrs863223906
Varsomers863223906
Maprs863223906
PheGenIrs863223906
hapmaprs863223906
1000 genomesrs863223906
hgdprs863223906
ensemblrs863223906
gopubmedrs863223906
geneviewrs863223906
scholarrs863223906
googlers863223906
pharmgkbrs863223906
gwascentralrs863223906
openSNPrs863223906
23andMers863223906
23andMe allrs863223906
SNP Nexus

SNPshotrs863223906
SNPdbers863223906
MSV3drs863223906
GWAS Ctlgrs863223906
Max Magnitude0
ClinVar
Risk rs863223906(G;G)
Alt rs863223906(G;G)
Reference rs863223906(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene ALAS2
CLNDBN not provided
Reversed 1
HGVS NC_000023.10:g.55035678T>C
CLNSRC
CLNACC RCV000195971.1,