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rs147455037

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs147455037(C;T)
Make rs147455037(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome22
Position38113560
GenePLA2G6
is asnp
is mentioned by
dbSNPrs147455037
dbSNP (old)rs147455037
ClinGenrs147455037
ebirs147455037
HLIrs147455037
Exacrs147455037
Gnomadrs147455037
Varsomers147455037
Maprs147455037
PheGenIrs147455037
Biobankrs147455037
1000 genomesrs147455037
hgdprs147455037
ensemblrs147455037
gopubmedrs147455037
geneviewrs147455037
scholarrs147455037
googlers147455037
pharmgkbrs147455037
gwascentralrs147455037
openSNPrs147455037
23andMers147455037
23andMe allrs147455037
SNPshotrs147455037
SNPdbers147455037
MSV3drs147455037
GWAS Ctlgrs147455037
Max Magnitude0
ClinVar
Risk rs147455037(T;T)
Alt rs147455037(T;T)
Reference Rs147455037(C;C)
Significance Probable-Pathogenic
Disease Abnormality of brain morphology
Variation info
Gene PLA2G6
CLNDBN Abnormality of brain morphology
Reversed 0
HGVS NC_000022.10:g.38509567C>T
CLNSRC
CLNACC RCV000454205.1,