Have questions? Visit https://www.reddit.com/r/SNPedia

rs786205655

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs786205655(C;T)
Make rs786205655(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome7
Position92503091
GenePEX1
is asnp
is mentioned by
dbSNPrs786205655
ebirs786205655
HLIrs786205655
Exacrs786205655
Varsomers786205655
Maprs786205655
PheGenIrs786205655
hapmaprs786205655
1000 genomesrs786205655
hgdprs786205655
ensemblrs786205655
gopubmedrs786205655
geneviewrs786205655
scholarrs786205655
googlers786205655
pharmgkbrs786205655
gwascentralrs786205655
openSNPrs786205655
23andMers786205655
23andMe allrs786205655
SNP Nexus

SNPshotrs786205655
SNPdbers786205655
MSV3drs786205655
GWAS Ctlgrs786205655
Max Magnitude0
ClinVar
Risk rs786205655(T;T)
Alt rs786205655(T;T)
Reference rs786205655(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene PEX1
CLNDBN not provided
Reversed 1
HGVS NC_000007.13:g.92132405G>A
CLNSRC
CLNACC RCV000171529.1,