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rs144896612

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs144896612(C;C)
Make rs144896612(C;T)
ReferenceGRCh38.p2 38.2/146
Chromosome6
Position87518711
GeneRARS2
is asnp
is mentioned by
dbSNPrs144896612
ebirs144896612
HLIrs144896612
Exacrs144896612
Varsomers144896612
Maprs144896612
PheGenIrs144896612
hapmaprs144896612
1000 genomesrs144896612
hgdprs144896612
ensemblrs144896612
gopubmedrs144896612
geneviewrs144896612
scholarrs144896612
googlers144896612
pharmgkbrs144896612
gwascentralrs144896612
openSNPrs144896612
23andMers144896612
23andMe allrs144896612
SNP Nexus

SNPshotrs144896612
SNPdbers144896612
MSV3drs144896612
GWAS Ctlgrs144896612
Max Magnitude0
ClinVar
Risk rs144896612(C;C)
Alt rs144896612(C;C)
Reference rs144896612(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene RARS2
CLNDBN not provided
Reversed 0
HGVS NC_000006.11:g.88228429T>C
CLNSRC
CLNACC RCV000195702.1,