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rs771895449

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(AG;AG) 0 common in clinvar
Make rs771895449(-;-)
Make rs771895449(-;AG)
ReferenceGRCh38.p7 38.3/150
Chromosome8
Position38145983
GeneSTAR
is asnp
is mentioned by
dbSNPrs771895449
dbSNP (classic)rs771895449
ClinGenrs771895449
ebirs771895449
HLIrs771895449
Exacrs771895449
Gnomadrs771895449
Varsomers771895449
LitVarrs771895449
Maprs771895449
PheGenIrs771895449
Biobankrs771895449
1000 genomesrs771895449
hgdprs771895449
ensemblrs771895449
geneviewrs771895449
scholarrs771895449
googlers771895449
pharmgkbrs771895449
gwascentralrs771895449
openSNPrs771895449
23andMers771895449
23andMe allrs771895449
SNPshotrs771895449
SNPdbers771895449
MSV3drs771895449
GWAS Ctlgrs771895449
Max Magnitude0
ClinVar
Risk rs771895449(-;-)
Alt rs771895449(-;-)
Reference Rs771895449(AG;AG)
Significance Probable-Pathogenic
Disease Cholesterol monooxygenase (side-chain cleaving) deficiency
Variation info
Gene STAR
CLNDBN Cholesterol monooxygenase (side-chain cleaving) deficiency
Reversed 0
HGVS NC_000008.10:g.38003501_38003502delAG
CLNSRC
CLNACC RCV000410363.1,