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

rs61750423

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs61750423(-;-)
Make rs61750423(-;A)
ReferenceGRCh38.p2 38.2/144
Chromosome7
Position92496766
GenePEX1
is asnp
is mentioned by
dbSNPrs61750423
ebirs61750423
HLIrs61750423
Exacrs61750423
Varsomers61750423
Maprs61750423
PheGenIrs61750423
hapmaprs61750423
1000 genomesrs61750423
hgdprs61750423
ensemblrs61750423
gopubmedrs61750423
geneviewrs61750423
scholarrs61750423
googlers61750423
pharmgkbrs61750423
gwascentralrs61750423
openSNPrs61750423
23andMers61750423
23andMe allrs61750423
SNP Nexus

SNPshotrs61750423
SNPdbers61750423
MSV3drs61750423
GWAS Ctlgrs61750423
Max Magnitude0
ClinVar
Risk rs61750423(;)
Alt rs61750423(;)
Reference rs61750423(A;A)
Significance Probable-Pathogenic
Disease Zellweger syndrome
Variation info
Gene PEX1
CLNDBN Zellweger syndrome
Reversed 1
HGVS NC_000007.13:g.92126080delT
CLNSRC
CLNACC RCV000169346.1,