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rs775065697

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs775065697(A;G)
Make rs775065697(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome6
Position44303159
GeneAARS2
is asnp
is mentioned by
dbSNPrs775065697
ebirs775065697
HLIrs775065697
Exacrs775065697
Varsomers775065697
Maprs775065697
PheGenIrs775065697
hapmaprs775065697
1000 genomesrs775065697
hgdprs775065697
ensemblrs775065697
gopubmedrs775065697
geneviewrs775065697
scholarrs775065697
googlers775065697
pharmgkbrs775065697
gwascentralrs775065697
openSNPrs775065697
23andMers775065697
23andMe allrs775065697
SNP Nexus

SNPshotrs775065697
SNPdbers775065697
MSV3drs775065697
GWAS Ctlgrs775065697
Max Magnitude0
ClinVar
Risk rs775065697(G;G)
Alt rs775065697(G;G)
Reference rs775065697(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene AARS2
CLNDBN not provided
Reversed 0
HGVS NC_000006.11:g.44270896A>G
CLNSRC
CLNACC RCV000196157.1,