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rs368497893

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs368497893(C;T)
Make rs368497893(T;T)
ReferenceGRCh38.p7 38.3/149
Chromosome22
Position38132831
GenePLA2G6
is asnp
is mentioned by
dbSNPrs368497893
dbSNP (classic)rs368497893
ClinGenrs368497893
ebirs368497893
HLIrs368497893
Exacrs368497893
Gnomadrs368497893
Varsomers368497893
LitVarrs368497893
Maprs368497893
PheGenIrs368497893
Biobankrs368497893
1000 genomesrs368497893
hgdprs368497893
ensemblrs368497893
geneviewrs368497893
scholarrs368497893
googlers368497893
pharmgkbrs368497893
gwascentralrs368497893
openSNPrs368497893
23andMers368497893
SNPshotrs368497893
SNPdbers368497893
MSV3drs368497893
GWAS Ctlgrs368497893
Max Magnitude0
ClinVar
Risk rs368497893(T;T)
Alt rs368497893(T;T)
Reference Rs368497893(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene PLA2G6
CLNDBN not provided
Reversed 0
HGVS NC_000022.10:g.38528838C>T
CLNSRC
CLNACC RCV000266508.1,