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rs886043708

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(CCAGTAT;CCAGTAT) 0 common in clinvar
Chromosome5
Position119527148
GeneHSD17B4
is asnp
is mentioned by
dbSNPrs886043708
dbSNP (classic)rs886043708
ClinGenrs886043708
ebirs886043708
HLIrs886043708
Exacrs886043708
Gnomadrs886043708
Varsomers886043708
LitVarrs886043708
Maprs886043708
PheGenIrs886043708
Biobankrs886043708
1000 genomesrs886043708
hgdprs886043708
ensemblrs886043708
geneviewrs886043708
scholarrs886043708
googlers886043708
pharmgkbrs886043708
gwascentralrs886043708
openSNPrs886043708
23andMers886043708
SNPshotrs886043708
SNPdbers886043708
MSV3drs886043708
GWAS Ctlgrs886043708
Max Magnitude0
ClinVar
Risk rs886043708(AA;AA)
Alt rs886043708(AA;AA)
Reference Rs886043708(CCAGTAT;CCAGTAT)
Significance Pathogenic
Disease Bifunctional peroxisomal enzyme deficiency
Variation info
Gene HSD17B4
CLNDBN Bifunctional peroxisomal enzyme deficiency
Reversed 0
HGVS NC_000005.9:g.118862843_118862849delCCAGTATinsAA
CLNSRC
CLNACC RCV000303201.1,