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rs61750414

From SNPedia

Orientationminus
Geno Mag Summary
(TC;TC) 0 common in clinvar
Make rs61750414(-;-)
Make rs61750414(-;TC)
ReferenceGRCh38.p2 38.2/144
Chromosome7
Position92501914
GenePEX1
is asnp
is mentioned by
dbSNPrs61750414
ebirs61750414
HLIrs61750414
Exacrs61750414
Varsomers61750414
Maprs61750414
PheGenIrs61750414
hapmaprs61750414
1000 genomesrs61750414
hgdprs61750414
ensemblrs61750414
gopubmedrs61750414
geneviewrs61750414
scholarrs61750414
googlers61750414
pharmgkbrs61750414
gwascentralrs61750414
openSNPrs61750414
23andMers61750414
23andMe allrs61750414
SNP Nexus

SNPshotrs61750414
SNPdbers61750414
MSV3drs61750414
GWAS Ctlgrs61750414
Max Magnitude0
ClinVar
Risk rs61750414(;)
Alt rs61750414(;)
Reference rs61750414(TC;TC)
Significance Probable-Pathogenic
Disease Zellweger syndrome
Variation info
Gene PEX1
CLNDBN Zellweger syndrome
Reversed 1
HGVS NC_000007.13:g.92131228_92131229delGA
CLNSRC
CLNACC RCV000169203.1,