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rs772887102

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs772887102(A;C)
Make rs772887102(C;C)
ReferenceGRCh38.p2 38.2/146
Chromosome6
Position87548623
GeneRARS2
is asnp
is mentioned by
dbSNPrs772887102
ebirs772887102
HLIrs772887102
Exacrs772887102
Varsomers772887102
Maprs772887102
PheGenIrs772887102
hapmaprs772887102
1000 genomesrs772887102
hgdprs772887102
ensemblrs772887102
gopubmedrs772887102
geneviewrs772887102
scholarrs772887102
googlers772887102
pharmgkbrs772887102
gwascentralrs772887102
openSNPrs772887102
23andMers772887102
23andMe allrs772887102
SNP Nexus

SNPshotrs772887102
SNPdbers772887102
MSV3drs772887102
GWAS Ctlgrs772887102
Max Magnitude0
ClinVar
Risk rs772887102(C;C)
Alt rs772887102(C;C)
Reference rs772887102(A;A)
Significance Probable-Pathogenic
Disease not provided Inborn genetic diseases
Variation info
Gene RARS2
CLNDBN not provided Inborn genetic diseases
Reversed 0
HGVS NC_000006.11:g.88258341A>C
CLNSRC
CLNACC RCV000200004.2, RCV000210707.1,