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rs786205502

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs786205502(C;T)
Make rs786205502(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome17
Position35577102
GenePEX12
is asnp
is mentioned by
dbSNPrs786205502
ebirs786205502
HLIrs786205502
Exacrs786205502
Varsomers786205502
Maprs786205502
PheGenIrs786205502
hapmaprs786205502
1000 genomesrs786205502
hgdprs786205502
ensemblrs786205502
gopubmedrs786205502
geneviewrs786205502
scholarrs786205502
googlers786205502
pharmgkbrs786205502
gwascentralrs786205502
openSNPrs786205502
23andMers786205502
23andMe allrs786205502
SNP Nexus

SNPshotrs786205502
SNPdbers786205502
MSV3drs786205502
GWAS Ctlgrs786205502
Max Magnitude0
ClinVar
Risk rs786205502(T;T)
Alt rs786205502(T;T)
Reference rs786205502(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene PEX12
CLNDBN not provided
Reversed 1
HGVS NC_000017.10:g.33904121G>A
CLNSRC
CLNACC RCV000171253.1,