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rs786205656

From SNPedia

Orientationminus
Geno Mag Summary
(GTCA;GTCA) 0 common in clinvar
Make rs786205656(-;-)
Make rs786205656(-;GTCA)
ReferenceGRCh38.p2 38.2/146
Chromosome7
Position92517855
GenePEX1
is asnp
is mentioned by
dbSNPrs786205656
ebirs786205656
HLIrs786205656
Exacrs786205656
Varsomers786205656
Maprs786205656
PheGenIrs786205656
hapmaprs786205656
1000 genomesrs786205656
hgdprs786205656
ensemblrs786205656
gopubmedrs786205656
geneviewrs786205656
scholarrs786205656
googlers786205656
pharmgkbrs786205656
gwascentralrs786205656
openSNPrs786205656
23andMers786205656
23andMe allrs786205656
SNP Nexus

SNPshotrs786205656
SNPdbers786205656
MSV3drs786205656
GWAS Ctlgrs786205656
Max Magnitude0
ClinVar
Risk rs786205656(;)
Alt rs786205656(;)
Reference rs786205656(GTCA;GTCA)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene PEX1
CLNDBN not provided
Reversed 1
HGVS NC_000007.13:g.92147169_92147172delTGAC
CLNSRC
CLNACC RCV000171530.1,