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rs768344665

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs768344665(-;-)
Make rs768344665(-;T)
ReferenceGRCh38.p7 38.3/150
Chromosome12
Position32754023
GeneYARS2
is asnp
is mentioned by
dbSNPrs768344665
dbSNP (classic)rs768344665
ClinGenrs768344665
ebirs768344665
HLIrs768344665
Exacrs768344665
Gnomadrs768344665
Varsomers768344665
LitVarrs768344665
Maprs768344665
PheGenIrs768344665
Biobankrs768344665
1000 genomesrs768344665
hgdprs768344665
ensemblrs768344665
geneviewrs768344665
scholarrs768344665
googlers768344665
pharmgkbrs768344665
gwascentralrs768344665
openSNPrs768344665
23andMers768344665
SNPshotrs768344665
SNPdbers768344665
MSV3drs768344665
GWAS Ctlgrs768344665
Max Magnitude0
ClinVar
Risk rs768344665(-;-)
Alt rs768344665(-;-)
Reference Rs768344665(T;T)
Significance Pathogenic
Disease not provided
Variation info
Gene YARS2
CLNDBN not provided
Reversed 0
HGVS NC_000012.11:g.32906957delT
CLNSRC
CLNACC RCV000479623.1,