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rs863224186

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs863224186(C;T)
Make rs863224186(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome6
Position87529648
GeneRARS2
is asnp
is mentioned by
dbSNPrs863224186
ebirs863224186
HLIrs863224186
Exacrs863224186
Varsomers863224186
Maprs863224186
PheGenIrs863224186
hapmaprs863224186
1000 genomesrs863224186
hgdprs863224186
ensemblrs863224186
gopubmedrs863224186
geneviewrs863224186
scholarrs863224186
googlers863224186
pharmgkbrs863224186
gwascentralrs863224186
openSNPrs863224186
23andMers863224186
23andMe allrs863224186
SNP Nexus

SNPshotrs863224186
SNPdbers863224186
MSV3drs863224186
GWAS Ctlgrs863224186
Max Magnitude0
ClinVar
Risk rs863224186(T;T)
Alt rs863224186(T;T)
Reference rs863224186(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene RARS2
CLNDBN not provided
Reversed 1
HGVS NC_000006.11:g.88239366G>A
CLNSRC
CLNACC RCV000196151.1,