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rs863223862

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs863223862(A;A)
Make rs863223862(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome6
Position44307020
GeneAARS2, LOC105375073
is asnp
is mentioned by
dbSNPrs863223862
ebirs863223862
HLIrs863223862
Exacrs863223862
Varsomers863223862
Maprs863223862
PheGenIrs863223862
hapmaprs863223862
1000 genomesrs863223862
hgdprs863223862
ensemblrs863223862
gopubmedrs863223862
geneviewrs863223862
scholarrs863223862
googlers863223862
pharmgkbrs863223862
gwascentralrs863223862
openSNPrs863223862
23andMers863223862
23andMe allrs863223862
SNP Nexus

SNPshotrs863223862
SNPdbers863223862
MSV3drs863223862
GWAS Ctlgrs863223862
Max Magnitude0
ClinVar
Risk rs863223862(A;A)
Alt rs863223862(A;A)
Reference rs863223862(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene AARS2
CLNDBN not provided
Reversed 1
HGVS NC_000006.11:g.44274757C>T
CLNSRC
CLNACC RCV000199473.2,