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rs121908686

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121908686(A;A)
Make rs121908686(A;G)
ReferenceGRCh38 38.1/141
Chromosome22
Position38112558
GeneBAIAP2L2, PLA2G6
is asnp
is mentioned by
dbSNPrs121908686
ebirs121908686
HLIrs121908686
Exacrs121908686
Varsomers121908686
Maprs121908686
PheGenIrs121908686
hapmaprs121908686
1000 genomesrs121908686
hgdprs121908686
ensemblrs121908686
gopubmedrs121908686
geneviewrs121908686
scholarrs121908686
googlers121908686
pharmgkbrs121908686
gwascentralrs121908686
openSNPrs121908686
23andMers121908686
23andMe allrs121908686
SNP Nexus

SNPshotrs121908686
SNPdbers121908686
MSV3drs121908686
GWAS Ctlgrs121908686
Max Magnitude0
OMIM603604
Desc
Variant0009
Relatedalso
ClinVar
Risk rs121908686(A;A)
Alt rs121908686(A;A)
Reference rs121908686(G;G)
Significance Pathogenic
Disease Parkinson disease 14
Variation info
Gene BAIAP2L2 PLA2G6
CLNDBN Parkinson disease 14
Reversed 1
HGVS NC_000022.10:g.38508565C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000006581.2,