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rs878853044

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs878853044(-;-)
Make rs878853044(-;T)
ReferenceGRCh38.p2 38.2/147
Chromosome1
Position2408714
GenePEX10
is asnp
is mentioned by
dbSNPrs878853044
ebirs878853044
HLIrs878853044
Exacrs878853044
Varsomers878853044
Maprs878853044
PheGenIrs878853044
hapmaprs878853044
1000 genomesrs878853044
hgdprs878853044
ensemblrs878853044
gopubmedrs878853044
geneviewrs878853044
scholarrs878853044
googlers878853044
pharmgkbrs878853044
gwascentralrs878853044
openSNPrs878853044
23andMers878853044
23andMe allrs878853044
SNP Nexus

SNPshotrs878853044
SNPdbers878853044
MSV3drs878853044
GWAS Ctlgrs878853044
Max Magnitude0
ClinVar
Risk rs878853044(;)
Alt rs878853044(;)
Reference rs878853044(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene PEX10
CLNDBN not provided
Reversed 1
HGVS NC_000001.10:g.2340153delA
CLNSRC
CLNACC RCV000224922.1,