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rs863224181

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs863224181(A;A)
Make rs863224181(A;C)
ReferenceGRCh38.p2 38.2/146
Chromosome6
Position87514493
GeneRARS2
is asnp
is mentioned by
dbSNPrs863224181
ebirs863224181
HLIrs863224181
Exacrs863224181
Varsomers863224181
Maprs863224181
PheGenIrs863224181
hapmaprs863224181
1000 genomesrs863224181
hgdprs863224181
ensemblrs863224181
gopubmedrs863224181
geneviewrs863224181
scholarrs863224181
googlers863224181
pharmgkbrs863224181
gwascentralrs863224181
openSNPrs863224181
23andMers863224181
23andMe allrs863224181
SNP Nexus

SNPshotrs863224181
SNPdbers863224181
MSV3drs863224181
GWAS Ctlgrs863224181
Max Magnitude0
ClinVar
Risk rs863224181(A;A)
Alt rs863224181(A;A)
Reference rs863224181(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene RARS2
CLNDBN not provided
Reversed 1
HGVS NC_000006.11:g.88224211G>T
CLNSRC
CLNACC RCV000195917.1,