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rs869312935

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs869312935(C;C)
Make rs869312935(C;G)
ReferenceGRCh38.p2 38.2/147
Chromosome1
Position2406719
GenePEX10
is asnp
is mentioned by
dbSNPrs869312935
ebirs869312935
HLIrs869312935
Exacrs869312935
Varsomers869312935
Maprs869312935
PheGenIrs869312935
hapmaprs869312935
1000 genomesrs869312935
hgdprs869312935
ensemblrs869312935
gopubmedrs869312935
geneviewrs869312935
scholarrs869312935
googlers869312935
pharmgkbrs869312935
gwascentralrs869312935
openSNPrs869312935
23andMers869312935
23andMe allrs869312935
SNP Nexus

SNPshotrs869312935
SNPdbers869312935
MSV3drs869312935
GWAS Ctlgrs869312935
Max Magnitude0
ClinVar
Risk rs869312935(C;C)
Alt rs869312935(C;C)
Reference rs869312935(G;G)
Significance Pathogenic
Disease Inborn genetic diseases
Variation info
Gene PEX10
CLNDBN Inborn genetic diseases
Reversed 1
HGVS NC_000001.10:g.2338158C>G
CLNSRC
CLNACC RCV000210672.1,