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rs786205586

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs786205586(C;C)
Make rs786205586(C;T)
ReferenceGRCh38.p2 38.2/146
Chromosome7
Position92494519
GenePEX1
is asnp
is mentioned by
dbSNPrs786205586
ebirs786205586
HLIrs786205586
Exacrs786205586
Varsomers786205586
Maprs786205586
PheGenIrs786205586
hapmaprs786205586
1000 genomesrs786205586
hgdprs786205586
ensemblrs786205586
gopubmedrs786205586
geneviewrs786205586
scholarrs786205586
googlers786205586
pharmgkbrs786205586
gwascentralrs786205586
openSNPrs786205586
23andMers786205586
23andMe allrs786205586
SNP Nexus

SNPshotrs786205586
SNPdbers786205586
MSV3drs786205586
GWAS Ctlgrs786205586
Max Magnitude0
ClinVar
Risk rs786205586(C;C)
Alt rs786205586(C;C)
Reference rs786205586(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene PEX1
CLNDBN not provided
Reversed 1
HGVS NC_000007.13:g.92123833A>G
CLNSRC
CLNACC RCV000171408.1,