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rs148921184

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs148921184(A;A)
Make rs148921184(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome6
Position5771341
GeneFARS2
is asnp
is mentioned by
dbSNPrs148921184
ebirs148921184
HLIrs148921184
Exacrs148921184
Varsomers148921184
Maprs148921184
PheGenIrs148921184
hapmaprs148921184
1000 genomesrs148921184
hgdprs148921184
ensemblrs148921184
gopubmedrs148921184
geneviewrs148921184
scholarrs148921184
googlers148921184
pharmgkbrs148921184
gwascentralrs148921184
openSNPrs148921184
23andMers148921184
23andMe allrs148921184
SNP Nexus

SNPshotrs148921184
SNPdbers148921184
MSV3drs148921184
GWAS Ctlgrs148921184
Max Magnitude0
ClinVar
Risk rs148921184(A;A)
Alt rs148921184(A;A)
Reference rs148921184(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene FARS2
CLNDBN not provided
Reversed 0
HGVS NC_000006.11:g.5771574G>A
CLNSRC
CLNACC RCV000198469.1,