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rs863224182

From SNPedia

Orientationminus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs863224182(-;G)
Make rs863224182(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome6
Position87524632
GeneRARS2
is asnp
is mentioned by
dbSNPrs863224182
ClinGenrs863224182
ebirs863224182
HLIrs863224182
Exacrs863224182
Varsomers863224182
Maprs863224182
PheGenIrs863224182
hapmaprs863224182
1000 genomesrs863224182
hgdprs863224182
ensemblrs863224182
gopubmedrs863224182
geneviewrs863224182
scholarrs863224182
googlers863224182
pharmgkbrs863224182
gwascentralrs863224182
openSNPrs863224182
23andMers863224182
23andMe allrs863224182
SNP Nexus

SNPshotrs863224182
SNPdbers863224182
MSV3drs863224182
GWAS Ctlgrs863224182
Max Magnitude0
ClinVar
Risk rs863224182(G;G)
Alt rs863224182(G;G)
Reference Rs863224182(;)
Significance Pathogenic
Disease not provided
Variation info
Gene RARS2
CLNDBN not provided
Reversed 1
HGVS NC_000006.11:g.88234351dupC
CLNSRC
CLNACC RCV000199506.1,