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rs587777772

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587777772(A;A)
Make rs587777772(A;G)
ReferenceGRCh38 38.1/142
Chromosome5
Position36200275
GeneNADK2
is asnp
is mentioned by
dbSNPrs587777772
ebirs587777772
HLIrs587777772
Exacrs587777772
Varsomers587777772
Maprs587777772
PheGenIrs587777772
hapmaprs587777772
1000 genomesrs587777772
hgdprs587777772
ensemblrs587777772
gopubmedrs587777772
geneviewrs587777772
scholarrs587777772
googlers587777772
pharmgkbrs587777772
gwascentralrs587777772
openSNPrs587777772
23andMers587777772
23andMe allrs587777772
SNP Nexus

SNPshotrs587777772
SNPdbers587777772
MSV3drs587777772
GWAS Ctlgrs587777772
Max Magnitude0
ClinVar
Risk rs587777772(A;A)
Alt rs587777772(A;A)
Reference rs587777772(G;G)
Significance Pathogenic
Disease 2
Variation info
Gene NADK2
CLNDBN 2,4-Dienoyl-CoA reductase deficiency
Reversed 0
HGVS NC_000005.9:g.36200377G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000144251.2,