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rs863224180

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs863224180(A;A)
Make rs863224180(A;T)
ReferenceGRCh38.p2 38.2/146
Chromosome6
Position87519609
GeneRARS2
is asnp
is mentioned by
dbSNPrs863224180
ebirs863224180
HLIrs863224180
Exacrs863224180
Varsomers863224180
Maprs863224180
PheGenIrs863224180
hapmaprs863224180
1000 genomesrs863224180
hgdprs863224180
ensemblrs863224180
gopubmedrs863224180
geneviewrs863224180
scholarrs863224180
googlers863224180
pharmgkbrs863224180
gwascentralrs863224180
openSNPrs863224180
23andMers863224180
23andMe allrs863224180
SNP Nexus

SNPshotrs863224180
SNPdbers863224180
MSV3drs863224180
GWAS Ctlgrs863224180
Max Magnitude0
ClinVar
Risk rs863224180(A;A)
Alt rs863224180(A;A)
Reference rs863224180(T;T)
Significance Pathogenic
Disease not provided
Variation info
Gene RARS2
CLNDBN not provided
Reversed 1
HGVS NC_000006.11:g.88229327A>T
CLNSRC
CLNACC RCV000199270.1,