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rs757743894

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(TTT;TTT) 0 common in clinvar
Make rs757743894(-;-)
Make rs757743894(-;TTT)
ReferenceGRCh38.p2 38.2/146
Chromosome6
Position87545677
GeneRARS2
is asnp
is mentioned by
dbSNPrs757743894
dbSNP (old)rs757743894
ClinGenrs757743894
ebirs757743894
HLIrs757743894
Exacrs757743894
Gnomadrs757743894
Varsomers757743894
Maprs757743894
PheGenIrs757743894
Biobankrs757743894
1000 genomesrs757743894
hgdprs757743894
ensemblrs757743894
gopubmedrs757743894
geneviewrs757743894
scholarrs757743894
googlers757743894
pharmgkbrs757743894
gwascentralrs757743894
openSNPrs757743894
23andMers757743894
23andMe allrs757743894
SNP Nexus

SNPshotrs757743894
SNPdbers757743894
MSV3drs757743894
GWAS Ctlgrs757743894
Max Magnitude0
ClinVar
Risk rs757743894(-;-)
Alt rs757743894(-;-)
Reference Rs757743894(TTT;TTT)
Significance Pathogenic
Disease not provided
Variation info
Gene RARS2
CLNDBN not provided
Reversed 0
HGVS NC_000006.11:g.88255395_88255397delTTT
CLNSRC
CLNACC RCV000199643.1,