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rs863223890

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs863223890(G;T)
Make rs863223890(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome18
Position12337522
GeneAFG3L2
is asnp
is mentioned by
dbSNPrs863223890
ClinGenrs863223890
ebirs863223890
HLIrs863223890
Exacrs863223890
Varsomers863223890
Maprs863223890
PheGenIrs863223890
hapmaprs863223890
1000 genomesrs863223890
hgdprs863223890
ensemblrs863223890
gopubmedrs863223890
geneviewrs863223890
scholarrs863223890
googlers863223890
pharmgkbrs863223890
gwascentralrs863223890
openSNPrs863223890
23andMers863223890
23andMe allrs863223890
SNP Nexus

SNPshotrs863223890
SNPdbers863223890
MSV3drs863223890
GWAS Ctlgrs863223890
Max Magnitude0
ClinVar
Risk rs863223890(T;T)
Alt rs863223890(T;T)
Reference Rs863223890(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene AFG3L2
CLNDBN not provided
Reversed 1
HGVS NC_000018.9:g.12337521C>A
CLNSRC
CLNACC RCV000198216.1,