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

rs863223891

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs863223891(A;A)
Make rs863223891(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome18
Position12356806
GeneAFG3L2
is asnp
is mentioned by
dbSNPrs863223891
ebirs863223891
HLIrs863223891
Exacrs863223891
Varsomers863223891
Maprs863223891
PheGenIrs863223891
hapmaprs863223891
1000 genomesrs863223891
hgdprs863223891
ensemblrs863223891
gopubmedrs863223891
geneviewrs863223891
scholarrs863223891
googlers863223891
pharmgkbrs863223891
gwascentralrs863223891
openSNPrs863223891
23andMers863223891
23andMe allrs863223891
SNP Nexus

SNPshotrs863223891
SNPdbers863223891
MSV3drs863223891
GWAS Ctlgrs863223891
Max Magnitude0
ClinVar
Risk rs863223891(A;A)
Alt rs863223891(A;A)
Reference rs863223891(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene AFG3L2
CLNDBN not provided
Reversed 1
HGVS NC_000018.9:g.12356805C>T
CLNSRC
CLNACC RCV000199195.1,