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

rs797044855

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs797044855(A;A)
Make rs797044855(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome7
Position30599995
GeneGARS
is asnp
is mentioned by
dbSNPrs797044855
ebirs797044855
HLIrs797044855
Exacrs797044855
Varsomers797044855
Maprs797044855
PheGenIrs797044855
hapmaprs797044855
1000 genomesrs797044855
hgdprs797044855
ensemblrs797044855
gopubmedrs797044855
geneviewrs797044855
scholarrs797044855
googlers797044855
pharmgkbrs797044855
gwascentralrs797044855
openSNPrs797044855
23andMers797044855
23andMe allrs797044855
SNP Nexus

SNPshotrs797044855
SNPdbers797044855
MSV3drs797044855
GWAS Ctlgrs797044855
Max Magnitude0
ClinVar
Risk rs797044855(A;A)
Alt rs797044855(A;A)
Reference rs797044855(G;G)
Significance Pathogenic
Disease Inborn genetic diseases
Variation info
Gene GARS
CLNDBN Inborn genetic diseases
Reversed 0
HGVS NC_000007.13:g.30639611G>A
CLNSRC
CLNACC RCV000190657.1,