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rs786205556

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs786205556(C;T)
Make rs786205556(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome22
Position18078604
GenePEX26
is asnp
is mentioned by
dbSNPrs786205556
ebirs786205556
HLIrs786205556
Exacrs786205556
Varsomers786205556
Maprs786205556
PheGenIrs786205556
hapmaprs786205556
1000 genomesrs786205556
hgdprs786205556
ensemblrs786205556
gopubmedrs786205556
geneviewrs786205556
scholarrs786205556
googlers786205556
pharmgkbrs786205556
gwascentralrs786205556
openSNPrs786205556
23andMers786205556
23andMe allrs786205556
SNP Nexus

SNPshotrs786205556
SNPdbers786205556
MSV3drs786205556
GWAS Ctlgrs786205556
Max Magnitude0
ClinVar
Risk rs786205556(T;T)
Alt rs786205556(T;T)
Reference rs786205556(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene PEX26
CLNDBN not provided
Reversed 0
HGVS NC_000022.10:g.18561370C>T
CLNSRC
CLNACC RCV000171354.1,