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rs200781477

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs200781477(C;C)
Make rs200781477(C;G)
ReferenceGRCh38.p2 38.2/146
Chromosome6
Position44301382
GeneAARS2
is asnp
is mentioned by
dbSNPrs200781477
ebirs200781477
HLIrs200781477
Exacrs200781477
Varsomers200781477
Maprs200781477
PheGenIrs200781477
hapmaprs200781477
1000 genomesrs200781477
hgdprs200781477
ensemblrs200781477
gopubmedrs200781477
geneviewrs200781477
scholarrs200781477
googlers200781477
pharmgkbrs200781477
gwascentralrs200781477
openSNPrs200781477
23andMers200781477
23andMe allrs200781477
SNP Nexus

SNPshotrs200781477
SNPdbers200781477
MSV3drs200781477
GWAS Ctlgrs200781477
Max Magnitude0
ClinVar
Risk rs200781477(C;C)
Alt rs200781477(C;C)
Reference rs200781477(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene AARS2
CLNDBN not provided
Reversed 0
HGVS NC_000006.11:g.44269119G>T
CLNSRC
CLNACC RCV000200375.1,