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rs121434634

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs121434634(C;C)
Make rs121434634(C;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position186894164
GenePLA2G4A
is asnp
is mentioned by
dbSNPrs121434634
ebirs121434634
HLIrs121434634
Exacrs121434634
Varsomers121434634
Maprs121434634
PheGenIrs121434634
hapmaprs121434634
1000 genomesrs121434634
hgdprs121434634
ensemblrs121434634
gopubmedrs121434634
geneviewrs121434634
scholarrs121434634
googlers121434634
pharmgkbrs121434634
gwascentralrs121434634
openSNPrs121434634
23andMers121434634
23andMe allrs121434634
SNP Nexus

SNPshotrs121434634
SNPdbers121434634
MSV3drs121434634
GWAS Ctlgrs121434634
Max Magnitude0
OMIM600522
Desc
Variant0001
Relatedalso
ClinVar
Risk rs121434634(C;C)
Alt rs121434634(C;C)
Reference rs121434634(T;T)
Significance Pathogenic
Disease Phospholipase a2
Variation info
Gene PLA2G4A
CLNDBN Phospholipase a2, group IV a, deficiency of
Reversed 0
HGVS NC_000001.10:g.186863296T>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000009647.2,