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rs61750422

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs61750422(C;T)
Make rs61750422(T;T)
ReferenceGRCh38.p7 38.3/149
Chromosome7
Position92499808
GenePEX1
is asnp
is mentioned by
dbSNPrs61750422
dbSNP (classic)rs61750422
ClinGenrs61750422
ebirs61750422
HLIrs61750422
Exacrs61750422
Gnomadrs61750422
Varsomers61750422
LitVarrs61750422
Maprs61750422
PheGenIrs61750422
Biobankrs61750422
1000 genomesrs61750422
hgdprs61750422
ensemblrs61750422
geneviewrs61750422
scholarrs61750422
googlers61750422
pharmgkbrs61750422
gwascentralrs61750422
openSNPrs61750422
23andMers61750422
23andMe allrs61750422
SNPshotrs61750422
SNPdbers61750422
MSV3drs61750422
GWAS Ctlgrs61750422
Max Magnitude0
ClinVar
Risk rs61750422(A;A) rs61750422(G;G) rs61750422(T;T)
Alt rs61750422(A;A) rs61750422(G;G) rs61750422(T;T)
Reference Rs61750422(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene PEX1
CLNDBN not provided
Reversed 1
HGVS NC_000007.13:g.92129122G>A
CLNSRC
CLNACC RCV000254886.1,