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rs1060499764

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1060499764(A;G)
Make rs1060499764(G;G)
ReferenceGRCh38.p7 38.3/150
Chromosome22
Position38120861
GenePLA2G6
is asnp
is mentioned by
dbSNPrs1060499764
dbSNP (classic)rs1060499764
ClinGenrs1060499764
ebirs1060499764
HLIrs1060499764
Exacrs1060499764
Gnomadrs1060499764
Varsomers1060499764
LitVarrs1060499764
Maprs1060499764
PheGenIrs1060499764
Biobankrs1060499764
1000 genomesrs1060499764
hgdprs1060499764
ensemblrs1060499764
geneviewrs1060499764
scholarrs1060499764
googlers1060499764
pharmgkbrs1060499764
gwascentralrs1060499764
openSNPrs1060499764
23andMers1060499764
23andMe allrs1060499764
SNPshotrs1060499764
SNPdbers1060499764
MSV3drs1060499764
GWAS Ctlgrs1060499764
Max Magnitude0
ClinVar
Risk rs1060499764(G;G)
Alt rs1060499764(G;G)
Reference Rs1060499764(A;A)
Significance Probable-Pathogenic
Disease Abnormality of brain morphology
Variation info
Gene PLA2G6
CLNDBN Abnormality of brain morphology
Reversed 1
HGVS NC_000022.10:g.38516868T>C
CLNSRC
CLNACC RCV000454298.1,