Have questions? Visit https://www.reddit.com/r/SNPedia

rs765044856

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs765044856(C;T)
Make rs765044856(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome6
Position87524578
GeneRARS2
is asnp
is mentioned by
dbSNPrs765044856
ebirs765044856
HLIrs765044856
Exacrs765044856
Varsomers765044856
Maprs765044856
PheGenIrs765044856
hapmaprs765044856
1000 genomesrs765044856
hgdprs765044856
ensemblrs765044856
gopubmedrs765044856
geneviewrs765044856
scholarrs765044856
googlers765044856
pharmgkbrs765044856
gwascentralrs765044856
openSNPrs765044856
23andMers765044856
23andMe allrs765044856
SNP Nexus

SNPshotrs765044856
SNPdbers765044856
MSV3drs765044856
GWAS Ctlgrs765044856
Max Magnitude0
ClinVar
Risk rs765044856(T;T)
Alt rs765044856(T;T)
Reference rs765044856(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene RARS2
CLNDBN not provided
Reversed 0
HGVS NC_000006.11:g.88234296C>T
CLNSRC
CLNACC RCV000197178.1,