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rs121909053

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121909053(A;A)
Make rs121909053(A;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position167825265
GeneSERPINI1
is asnp
is mentioned by
dbSNPrs121909053
ebirs121909053
HLIrs121909053
Exacrs121909053
Varsomers121909053
Maprs121909053
PheGenIrs121909053
hapmaprs121909053
1000 genomesrs121909053
hgdprs121909053
ensemblrs121909053
gopubmedrs121909053
geneviewrs121909053
scholarrs121909053
googlers121909053
pharmgkbrs121909053
gwascentralrs121909053
openSNPrs121909053
23andMers121909053
23andMe allrs121909053
SNP Nexus

SNPshotrs121909053
SNPdbers121909053
MSV3drs121909053
GWAS Ctlgrs121909053
Max Magnitude0
OMIM602445
Desc
Variant0004
Relatedalso
ClinVar
Risk rs121909053(A;A)
Alt rs121909053(A;A)
Reference rs121909053(G;G)
Significance Pathogenic
Disease Encephalopathy
Variation info
Gene SERPINI1
CLNDBN Encephalopathy, familial, with neuroserpin inclusion bodies
Reversed 0
HGVS NC_000003.11:g.167543053G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000007505.3,