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rs1057518618

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(AAAG;AAAG) 0 common in clinvar
Make rs1057518618(-;-)
Make rs1057518618(-;AAGA)
Make rs1057518618(AAGA;AAGA)
ReferenceGRCh38.p7 38.3/150
Chromosome5
Position168510677
GeneRARS
is asnp
is mentioned by
dbSNPrs1057518618
dbSNP (old)rs1057518618
ClinGenrs1057518618
ebirs1057518618
HLIrs1057518618
Exacrs1057518618
Gnomadrs1057518618
Varsomers1057518618
Maprs1057518618
PheGenIrs1057518618
Biobankrs1057518618
1000 genomesrs1057518618
hgdprs1057518618
ensemblrs1057518618
gopubmedrs1057518618
geneviewrs1057518618
scholarrs1057518618
googlers1057518618
pharmgkbrs1057518618
gwascentralrs1057518618
openSNPrs1057518618
23andMers1057518618
23andMe allrs1057518618
SNPshotrs1057518618
SNPdbers1057518618
MSV3drs1057518618
GWAS Ctlgrs1057518618
Max Magnitude0
ClinVar
Risk rs1057518618(-;-)
Alt rs1057518618(-;-)
Reference Rs1057518618(AAAG;AAAG)
Significance Pathogenic
Disease not provided
Variation info
Gene RARS
CLNDBN not provided
Reversed 0
HGVS NC_000005.9:g.167937682_167937685delAAGA
CLNSRC
CLNACC RCV000413106.1,