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rs121434635

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121434635(A;A)
Make rs121434635(A;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position186956219
GenePLA2G4A
is asnp
is mentioned by
dbSNPrs121434635
ebirs121434635
HLIrs121434635
Exacrs121434635
Varsomers121434635
Maprs121434635
PheGenIrs121434635
hapmaprs121434635
1000 genomesrs121434635
hgdprs121434635
ensemblrs121434635
gopubmedrs121434635
geneviewrs121434635
scholarrs121434635
googlers121434635
pharmgkbrs121434635
gwascentralrs121434635
openSNPrs121434635
23andMers121434635
23andMe allrs121434635
SNP Nexus

SNPshotrs121434635
SNPdbers121434635
MSV3drs121434635
GWAS Ctlgrs121434635
Max Magnitude0
OMIM600522
Desc
Variant0002
Relatedalso
ClinVar
Risk rs121434635(A;A)
Alt rs121434635(A;A)
Reference rs121434635(G;G)
Significance Pathogenic
Disease Phospholipase a2
Variation info
Gene PLA2G4A
CLNDBN Phospholipase a2, group IV a, deficiency of
Reversed 0
HGVS NC_000001.10:g.186925351G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000009648.3,