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rs747330606

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs747330606(G;T)
Make rs747330606(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome22
Position41515536
GeneACO2
is asnp
is mentioned by
dbSNPrs747330606
ebirs747330606
HLIrs747330606
Exacrs747330606
Varsomers747330606
Maprs747330606
PheGenIrs747330606
hapmaprs747330606
1000 genomesrs747330606
hgdprs747330606
ensemblrs747330606
gopubmedrs747330606
geneviewrs747330606
scholarrs747330606
googlers747330606
pharmgkbrs747330606
gwascentralrs747330606
openSNPrs747330606
23andMers747330606
23andMe allrs747330606
SNP Nexus

SNPshotrs747330606
SNPdbers747330606
MSV3drs747330606
GWAS Ctlgrs747330606
Max Magnitude0
ClinVar
Risk rs747330606(T;T)
Alt rs747330606(T;T)
Reference rs747330606(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene ACO2
CLNDBN not provided
Reversed 0
HGVS NC_000022.10:g.41911540G>T
CLNSRC
CLNACC RCV000200546.2,