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rs761368190

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs761368190(A;A)
Make rs761368190(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome22
Position41522872
GeneACO2
is asnp
is mentioned by
dbSNPrs761368190
ebirs761368190
HLIrs761368190
Exacrs761368190
Varsomers761368190
Maprs761368190
PheGenIrs761368190
hapmaprs761368190
1000 genomesrs761368190
hgdprs761368190
ensemblrs761368190
gopubmedrs761368190
geneviewrs761368190
scholarrs761368190
googlers761368190
pharmgkbrs761368190
gwascentralrs761368190
openSNPrs761368190
23andMers761368190
23andMe allrs761368190
SNP Nexus

SNPshotrs761368190
SNPdbers761368190
MSV3drs761368190
GWAS Ctlgrs761368190
Max Magnitude0
ClinVar
Risk rs761368190(A;A)
Alt rs761368190(A;A)
Reference rs761368190(G;G)
Significance Probable-Pathogenic
Disease Inborn genetic diseases
Variation info
Gene ACO2
CLNDBN Inborn genetic diseases
Reversed 0
HGVS NC_000022.10:g.41918876G>A
CLNSRC
CLNACC RCV000210720.1,