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rs766771165

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs766771165(-;A)
Make rs766771165(A;A)
ReferenceGRCh38.p2 38.2/146
Chromosome6
Position44307280
GeneAARS2, LOC105375073
is asnp
is mentioned by
dbSNPrs766771165
ClinGenrs766771165
ebirs766771165
HLIrs766771165
Exacrs766771165
Varsomers766771165
Maprs766771165
PheGenIrs766771165
hapmaprs766771165
1000 genomesrs766771165
hgdprs766771165
ensemblrs766771165
gopubmedrs766771165
geneviewrs766771165
scholarrs766771165
googlers766771165
pharmgkbrs766771165
gwascentralrs766771165
openSNPrs766771165
23andMers766771165
23andMe allrs766771165
SNP Nexus

SNPshotrs766771165
SNPdbers766771165
MSV3drs766771165
GWAS Ctlgrs766771165
Max Magnitude0
ClinVar
Risk rs766771165(A;A)
Alt rs766771165(A;A)
Reference Rs766771165(-;-)
Significance Pathogenic
Disease not provided
Variation info
Gene AARS2
CLNDBN not provided
Reversed 0
HGVS NC_000006.11:g.44275018dupA
CLNSRC
CLNACC RCV000199735.1,