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rs768351915

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs768351915(A;A)
Make rs768351915(A;C)
ReferenceGRCh38.p7 38.3/149
Chromosome6
Position44302059
GeneAARS2
is asnp
is mentioned by
dbSNPrs768351915
dbSNP (classic)rs768351915
ClinGenrs768351915
ebirs768351915
HLIrs768351915
Exacrs768351915
Gnomadrs768351915
Varsomers768351915
LitVarrs768351915
Maprs768351915
PheGenIrs768351915
Biobankrs768351915
1000 genomesrs768351915
hgdprs768351915
ensemblrs768351915
geneviewrs768351915
scholarrs768351915
googlers768351915
pharmgkbrs768351915
gwascentralrs768351915
openSNPrs768351915
23andMers768351915
23andMe allrs768351915
SNPshotrs768351915
SNPdbers768351915
MSV3drs768351915
GWAS Ctlgrs768351915
Max Magnitude0
ClinVar
Risk rs768351915(A;A)
Alt rs768351915(A;A)
Reference Rs768351915(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene AARS2
CLNDBN not provided
Reversed 0
HGVS NC_000006.11:g.44269796C>A
CLNSRC
CLNACC RCV000384046.1,