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

rs776158594

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs776158594(A;G)
Make rs776158594(G;G)
ReferenceGRCh38.p7 38.3/150
Chromosome22
Position50580356
GeneCHKB, CHKB-CPT1B, CPT1B
is asnp
is mentioned by
dbSNPrs776158594
dbSNP (classic)rs776158594
ClinGenrs776158594
ebirs776158594
HLIrs776158594
Exacrs776158594
Gnomadrs776158594
Varsomers776158594
LitVarrs776158594
Maprs776158594
PheGenIrs776158594
Biobankrs776158594
1000 genomesrs776158594
hgdprs776158594
ensemblrs776158594
geneviewrs776158594
scholarrs776158594
googlers776158594
pharmgkbrs776158594
gwascentralrs776158594
openSNPrs776158594
23andMers776158594
SNPshotrs776158594
SNPdbers776158594
MSV3drs776158594
GWAS Ctlgrs776158594
Max Magnitude0
ClinVar
Risk rs776158594(G;G)
Alt rs776158594(G;G)
Reference Rs776158594(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene CHKB-CPT1B CHKB CPT1B
CLNDBN not provided
Reversed 0
HGVS NC_000022.10:g.51018785A>G
CLNSRC
CLNACC RCV000494588.1,