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rs33917740

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs33917740(C;G)
Make rs33917740(G;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position167789149
GeneSERPINI1
is asnp
is mentioned by
dbSNPrs33917740
dbSNP (classic)rs33917740
ClinGenrs33917740
ebirs33917740
HLIrs33917740
Exacrs33917740
Gnomadrs33917740
Varsomers33917740
LitVarrs33917740
Maprs33917740
PheGenIrs33917740
Biobankrs33917740
1000 genomesrs33917740
hgdprs33917740
ensemblrs33917740
geneviewrs33917740
scholarrs33917740
googlers33917740
pharmgkbrs33917740
gwascentralrs33917740
openSNPrs33917740
23andMers33917740
SNPshotrs33917740
SNPdbers33917740
MSV3drs33917740
GWAS Ctlgrs33917740
GMAF0.1134
Max Magnitude0



ClinVar
Risk rs33917740(G;G)
Alt rs33917740(G;G)
Reference Rs33917740(C;C)
Significance Non-pathogenic
Disease Encephalopathy
Variation info
Gene SERPINI1
CLNDBN Encephalopathy, familial, with neuroserpin inclusion bodies
Reversed 0
HGVS NC_000003.11:g.167506937C>G
CLNSRC
CLNACC RCV000326135.1,