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rs863223889

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs863223889(A;A)
Make rs863223889(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome18
Position12358684
GeneAFG3L2
is asnp
is mentioned by
dbSNPrs863223889
ebirs863223889
HLIrs863223889
Exacrs863223889
Varsomers863223889
Maprs863223889
PheGenIrs863223889
hapmaprs863223889
1000 genomesrs863223889
hgdprs863223889
ensemblrs863223889
gopubmedrs863223889
geneviewrs863223889
scholarrs863223889
googlers863223889
pharmgkbrs863223889
gwascentralrs863223889
openSNPrs863223889
23andMers863223889
23andMe allrs863223889
SNP Nexus

SNPshotrs863223889
SNPdbers863223889
MSV3drs863223889
GWAS Ctlgrs863223889
Max Magnitude0
ClinVar
Risk rs863223889(A;A)
Alt rs863223889(A;A)
Reference rs863223889(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene AFG3L2
CLNDBN not provided
Reversed 1
HGVS NC_000018.9:g.12358683C>T
CLNSRC
CLNACC RCV000198799.1,