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rs3792683

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs3792683(A;G)
Make rs3792683(G;G)
ReferenceGRCh38 38.1/141
Chromosome4
Position99589746
GeneMTTP
is asnp
is mentioned by
dbSNPrs3792683
dbSNP (classic)rs3792683
ClinGenrs3792683
ebirs3792683
HLIrs3792683
Exacrs3792683
Gnomadrs3792683
Varsomers3792683
LitVarrs3792683
Maprs3792683
PheGenIrs3792683
Biobankrs3792683
1000 genomesrs3792683
hgdprs3792683
ensemblrs3792683
geneviewrs3792683
scholarrs3792683
googlers3792683
pharmgkbrs3792683
gwascentralrs3792683
openSNPrs3792683
23andMers3792683
SNPshotrs3792683
SNPdbers3792683
MSV3drs3792683
GWAS Ctlgrs3792683
GMAF0.123
Max Magnitude0
? (A;A) (A;G) (G;G) 28





ClinVar
Risk rs3792683(G;G)
Alt rs3792683(G;G)
Reference Rs3792683(A;A)
Significance Probable-non-pathogenic
Disease Abetalipoproteinemia
Variation info
Gene MTTP
CLNDBN Abetalipoproteinemia
Reversed 0
HGVS NC_000004.11:g.100510903A>G
CLNSRC
CLNACC RCV000376488.1,