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rs61750412

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(CA;CA) 0 common in clinvar
Make rs61750412(-;-)
Make rs61750412(-;CA)
ReferenceGRCh38.p7 38.3/150
Chromosome7
Position92504768
GenePEX1
is asnp
is mentioned by
dbSNPrs61750412
dbSNP (classic)rs61750412
ClinGenrs61750412
ebirs61750412
HLIrs61750412
Exacrs61750412
Gnomadrs61750412
Varsomers61750412
LitVarrs61750412
Maprs61750412
PheGenIrs61750412
Biobankrs61750412
1000 genomesrs61750412
hgdprs61750412
ensemblrs61750412
geneviewrs61750412
scholarrs61750412
googlers61750412
pharmgkbrs61750412
gwascentralrs61750412
openSNPrs61750412
23andMers61750412
23andMe allrs61750412
SNPshotrs61750412
SNPdbers61750412
MSV3drs61750412
GWAS Ctlgrs61750412
Max Magnitude0
ClinVar
Risk rs61750412(-;-)
Alt rs61750412(-;-)
Reference Rs61750412(CA;CA)
Significance Probable-Pathogenic
Disease Zellweger syndrome Peroxisome biogenesis disorder 1B
Variation info
Gene PEX1
CLNDBN Zellweger syndrome Peroxisome biogenesis disorder 1B
Reversed 1
HGVS NC_000007.13:g.92134082_92134083delTG
CLNSRC
CLNACC RCV000409983.1, RCV000411506.1,