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rs121908687

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121908687(C;T)
Make rs121908687(T;T)
ReferenceGRCh38 38.1/141
Chromosome22
Position38112541
GeneBAIAP2L2, PLA2G6
is asnp
is mentioned by
dbSNPrs121908687
ebirs121908687
HLIrs121908687
Exacrs121908687
Varsomers121908687
Maprs121908687
PheGenIrs121908687
hapmaprs121908687
1000 genomesrs121908687
hgdprs121908687
ensemblrs121908687
gopubmedrs121908687
geneviewrs121908687
scholarrs121908687
googlers121908687
pharmgkbrs121908687
gwascentralrs121908687
openSNPrs121908687
23andMers121908687
23andMe allrs121908687
SNP Nexus

SNPshotrs121908687
SNPdbers121908687
MSV3drs121908687
GWAS Ctlgrs121908687
Max Magnitude0
OMIM603604
Desc
Variant0010
Relatedalso
ClinVar
Risk rs121908687(T;T)
Alt rs121908687(T;T)
Reference rs121908687(C;C)
Significance Pathogenic
Disease Parkinson disease 14
Variation info
Gene BAIAP2L2 PLA2G6
CLNDBN Parkinson disease 14
Reversed 1
HGVS NC_000022.10:g.38508548G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000006582.4,