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rs786205580

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs786205580(G;T)
Make rs786205580(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome6
Position42978490
GenePEX6
is asnp
is mentioned by
dbSNPrs786205580
ebirs786205580
HLIrs786205580
Exacrs786205580
Varsomers786205580
Maprs786205580
PheGenIrs786205580
hapmaprs786205580
1000 genomesrs786205580
hgdprs786205580
ensemblrs786205580
gopubmedrs786205580
geneviewrs786205580
scholarrs786205580
googlers786205580
pharmgkbrs786205580
gwascentralrs786205580
openSNPrs786205580
23andMers786205580
23andMe allrs786205580
SNP Nexus

SNPshotrs786205580
SNPdbers786205580
MSV3drs786205580
GWAS Ctlgrs786205580
Max Magnitude0
ClinVar
Risk rs786205580(T;T)
Alt rs786205580(T;T)
Reference rs786205580(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene PEX6
CLNDBN not provided
Reversed 1
HGVS NC_000006.11:g.42946228C>A
CLNSRC
CLNACC RCV000171396.1,