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rs121908682

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs121908682(A;A)
Make rs121908682(A;T)
ReferenceGRCh38 38.1/141
Chromosome22
Position38132979
GenePLA2G6
is asnp
is mentioned by
dbSNPrs121908682
ebirs121908682
HLIrs121908682
Exacrs121908682
Varsomers121908682
Maprs121908682
PheGenIrs121908682
hapmaprs121908682
1000 genomesrs121908682
hgdprs121908682
ensemblrs121908682
gopubmedrs121908682
geneviewrs121908682
scholarrs121908682
googlers121908682
pharmgkbrs121908682
gwascentralrs121908682
openSNPrs121908682
23andMers121908682
23andMe allrs121908682
SNP Nexus

SNPshotrs121908682
SNPdbers121908682
MSV3drs121908682
GWAS Ctlgrs121908682
Max Magnitude0
OMIM603604
Desc
Variant0003
Relatedalso
ClinVar
Risk rs121908682(A;A)
Alt rs121908682(A;A)
Reference rs121908682(T;T)
Significance Pathogenic
Disease Infantile neuroaxonal dystrophy
Variation info
Gene PLA2G6
CLNDBN Infantile neuroaxonal dystrophy
Reversed 1
HGVS NC_000022.10:g.38528986A>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000006574.3,