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rs61750426

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs61750426(-;-)
Make rs61750426(-;A)
ReferenceGRCh38.p2 38.2/144
Chromosome7
Position92494497
GenePEX1
is asnp
is mentioned by
dbSNPrs61750426
ebirs61750426
HLIrs61750426
Exacrs61750426
Varsomers61750426
Maprs61750426
PheGenIrs61750426
hapmaprs61750426
1000 genomesrs61750426
hgdprs61750426
ensemblrs61750426
gopubmedrs61750426
geneviewrs61750426
scholarrs61750426
googlers61750426
pharmgkbrs61750426
gwascentralrs61750426
openSNPrs61750426
23andMers61750426
23andMe allrs61750426
SNP Nexus

SNPshotrs61750426
SNPdbers61750426
MSV3drs61750426
GWAS Ctlgrs61750426
Max Magnitude0
ClinVar
Risk rs61750426(;)
Alt rs61750426(;)
Reference rs61750426(A;A)
Significance Probable-Pathogenic
Disease Zellweger syndrome
Variation info
Gene PEX1
CLNDBN Zellweger syndrome
Reversed 1
HGVS NC_000007.13:g.92123811delT
CLNSRC
CLNACC RCV000169435.1,