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rs786204743

From SNPedia

Orientationminus
Geno Mag Summary
(CT;CT) 0 common in clinvar
Make rs786204743(-;-)
Make rs786204743(-;CT)
ReferenceGRCh38.p2 38.2/146
Chromosome7
Position92511029
GenePEX1
is asnp
is mentioned by
dbSNPrs786204743
ebirs786204743
HLIrs786204743
Exacrs786204743
Varsomers786204743
Maprs786204743
PheGenIrs786204743
hapmaprs786204743
1000 genomesrs786204743
hgdprs786204743
ensemblrs786204743
gopubmedrs786204743
geneviewrs786204743
scholarrs786204743
googlers786204743
pharmgkbrs786204743
gwascentralrs786204743
openSNPrs786204743
23andMers786204743
23andMe allrs786204743
SNP Nexus

SNPshotrs786204743
SNPdbers786204743
MSV3drs786204743
GWAS Ctlgrs786204743
Max Magnitude0
ClinVar
Risk rs786204743(;)
Alt rs786204743(;)
Reference rs786204743(CT;CT)
Significance Probable-Pathogenic
Disease Zellweger syndrome
Variation info
Gene PEX1
CLNDBN Zellweger syndrome
Reversed 1
HGVS NC_000007.13:g.92140343_92140344delAG
CLNSRC
CLNACC RCV000169592.1,