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rs374746113

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs374746113(A;G)
Make rs374746113(G;G)
ReferenceGRCh38.p7 38.3/150
Chromosome22
Position38145477
GenePLA2G6
is asnp
is mentioned by
dbSNPrs374746113
dbSNP (classic)rs374746113
ClinGenrs374746113
ebirs374746113
HLIrs374746113
Exacrs374746113
Gnomadrs374746113
Varsomers374746113
LitVarrs374746113
Maprs374746113
PheGenIrs374746113
Biobankrs374746113
1000 genomesrs374746113
hgdprs374746113
ensemblrs374746113
geneviewrs374746113
scholarrs374746113
googlers374746113
pharmgkbrs374746113
gwascentralrs374746113
openSNPrs374746113
23andMers374746113
SNPshotrs374746113
SNPdbers374746113
MSV3drs374746113
GWAS Ctlgrs374746113
Max Magnitude0
ClinVar
Risk rs374746113(G;G)
Alt rs374746113(G;G)
Reference Rs374746113(A;A)
Significance Probable-Pathogenic
Disease Iron accumulation in brain not provided
Variation info
Gene PLA2G6
CLNDBN Iron accumulation in brain not provided
Reversed 0
HGVS NC_000022.10:g.38541484A>G
CLNSRC
CLNACC RCV000147324.1, RCV000414098.1,