Have questions? Visit https://www.reddit.com/r/SNPedia

rs753489572

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs753489572(A;G)
Make rs753489572(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome14
Position73961499
GeneCOQ6, ENTPD5
is asnp
is mentioned by
dbSNPrs753489572
ebirs753489572
HLIrs753489572
Exacrs753489572
Varsomers753489572
Maprs753489572
PheGenIrs753489572
hapmaprs753489572
1000 genomesrs753489572
hgdprs753489572
ensemblrs753489572
gopubmedrs753489572
geneviewrs753489572
scholarrs753489572
googlers753489572
pharmgkbrs753489572
gwascentralrs753489572
openSNPrs753489572
23andMers753489572
23andMe allrs753489572
SNP Nexus

SNPshotrs753489572
SNPdbers753489572
MSV3drs753489572
GWAS Ctlgrs753489572
Max Magnitude0
ClinVar
Risk rs753489572(G;G)
Alt rs753489572(G;G)
Reference rs753489572(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene COQ6 ENTPD5
CLNDBN not provided
Reversed 0
HGVS NC_000014.8:g.74428202A>G
CLNSRC
CLNACC RCV000200596.1,