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rs757169781

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs757169781(A;T)
Make rs757169781(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome6
Position44313103
GeneAARS2
is asnp
is mentioned by
dbSNPrs757169781
ebirs757169781
HLIrs757169781
Exacrs757169781
Varsomers757169781
Maprs757169781
PheGenIrs757169781
hapmaprs757169781
1000 genomesrs757169781
hgdprs757169781
ensemblrs757169781
gopubmedrs757169781
geneviewrs757169781
scholarrs757169781
googlers757169781
pharmgkbrs757169781
gwascentralrs757169781
openSNPrs757169781
23andMers757169781
23andMe allrs757169781
SNP Nexus

SNPshotrs757169781
SNPdbers757169781
MSV3drs757169781
GWAS Ctlgrs757169781
Max Magnitude0
ClinVar
Risk rs757169781(T;T)
Alt rs757169781(T;T)
Reference rs757169781(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene AARS2
CLNDBN not provided
Reversed 0
HGVS NC_000006.11:g.44280840A>T
CLNSRC
CLNACC RCV000195876.1,