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rs556433569

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs556433569(C;C)
Make rs556433569(C;T)
ReferenceGRCh38.p2 38.2/146
Chromosome3
Position171644922
GenePLD1
is asnp
is mentioned by
dbSNPrs556433569
ebirs556433569
HLIrs556433569
Exacrs556433569
Varsomers556433569
Maprs556433569
PheGenIrs556433569
hapmaprs556433569
1000 genomesrs556433569
hgdprs556433569
ensemblrs556433569
gopubmedrs556433569
geneviewrs556433569
scholarrs556433569
googlers556433569
pharmgkbrs556433569
gwascentralrs556433569
openSNPrs556433569
23andMers556433569
23andMe allrs556433569
SNP Nexus

SNPshotrs556433569
SNPdbers556433569
MSV3drs556433569
GWAS Ctlgrs556433569
Max Magnitude0
ClinVar
Risk rs556433569(C;C)
Alt rs556433569(C;C)
Reference rs556433569(T;T)
Significance Probable-Pathogenic
Disease Inborn genetic diseases
Variation info
Gene PLD1
CLNDBN Inborn genetic diseases
Reversed 0
HGVS NC_000003.11:g.171362712T>C
CLNSRC
CLNACC RCV000190783.1,