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rs863224183

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs863224183(-;TT)
Make rs863224183(TT;TT)
ReferenceGRCh38.p2 38.2/146
Chromosome6
Position87516808
GeneRARS2
is asnp
is mentioned by
dbSNPrs863224183
ClinGenrs863224183
ebirs863224183
HLIrs863224183
Exacrs863224183
Varsomers863224183
Maprs863224183
PheGenIrs863224183
hapmaprs863224183
1000 genomesrs863224183
hgdprs863224183
ensemblrs863224183
gopubmedrs863224183
geneviewrs863224183
scholarrs863224183
googlers863224183
pharmgkbrs863224183
gwascentralrs863224183
openSNPrs863224183
23andMers863224183
23andMe allrs863224183
SNP Nexus

SNPshotrs863224183
SNPdbers863224183
MSV3drs863224183
GWAS Ctlgrs863224183
Max Magnitude0
ClinVar
Risk rs863224183(TT;TT)
Alt rs863224183(TT;TT)
Reference Rs863224183(-;-)
Significance Pathogenic
Disease not provided
Variation info
Gene RARS2
CLNDBN not provided
Reversed 1
HGVS NC_000006.11:g.88226527_88226528dupAA
CLNSRC
CLNACC RCV000196620.1,