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rs199835443

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs199835443(A;A)
Make rs199835443(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome6
Position87524588
GeneRARS2
is asnp
is mentioned by
dbSNPrs199835443
ebirs199835443
HLIrs199835443
Exacrs199835443
Varsomers199835443
Maprs199835443
PheGenIrs199835443
hapmaprs199835443
1000 genomesrs199835443
hgdprs199835443
ensemblrs199835443
gopubmedrs199835443
geneviewrs199835443
scholarrs199835443
googlers199835443
pharmgkbrs199835443
gwascentralrs199835443
openSNPrs199835443
23andMers199835443
23andMe allrs199835443
SNP Nexus

SNPshotrs199835443
SNPdbers199835443
MSV3drs199835443
GWAS Ctlgrs199835443
Max Magnitude0
ClinVar
Risk rs199835443(A,C;A,C)
Alt rs199835443(A,C;A,C)
Reference rs199835443(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene RARS2
CLNDBN not provided
Reversed 0
HGVS NC_000006.11:g.88234306G>A
CLNSRC
CLNACC RCV000200708.1,