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rs869312934

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs869312934(C;T)
Make rs869312934(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome1
Position160279842
GenePEX19
is asnp
is mentioned by
dbSNPrs869312934
ebirs869312934
HLIrs869312934
Exacrs869312934
Varsomers869312934
Maprs869312934
PheGenIrs869312934
hapmaprs869312934
1000 genomesrs869312934
hgdprs869312934
ensemblrs869312934
gopubmedrs869312934
geneviewrs869312934
scholarrs869312934
googlers869312934
pharmgkbrs869312934
gwascentralrs869312934
openSNPrs869312934
23andMers869312934
23andMe allrs869312934
SNP Nexus

SNPshotrs869312934
SNPdbers869312934
MSV3drs869312934
GWAS Ctlgrs869312934
Max Magnitude0
ClinVar
Risk rs869312934(T;T)
Alt rs869312934(T;T)
Reference rs869312934(C;C)
Significance Pathogenic
Disease Inborn genetic diseases
Variation info
Gene PEX19
CLNDBN Inborn genetic diseases
Reversed 1
HGVS NC_000001.10:g.160249632G>A
CLNSRC
CLNACC RCV000210599.1,