Have questions? Visit https://www.reddit.com/r/SNPedia

rs146064714

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs146064714(G;T)
Make rs146064714(T;T)
ReferenceGRCh38 38.1/141
Chromosome4
Position99622756
GeneMTTP
is asnp
is mentioned by
dbSNPrs146064714
ebirs146064714
HLIrs146064714
Exacrs146064714
Varsomers146064714
Maprs146064714
PheGenIrs146064714
hapmaprs146064714
1000 genomesrs146064714
hgdprs146064714
ensemblrs146064714
gopubmedrs146064714
geneviewrs146064714
scholarrs146064714
googlers146064714
pharmgkbrs146064714
gwascentralrs146064714
openSNPrs146064714
23andMers146064714
23andMe allrs146064714
SNP Nexus

SNPshotrs146064714
SNPdbers146064714
MSV3drs146064714
GWAS Ctlgrs146064714
Max Magnitude0
ClinVar
Risk rs146064714(T;T)
Alt rs146064714(T;T)
Reference rs146064714(G;G)
Significance Pathogenic
Disease Abetalipoproteinaemia
Variation info
Gene MTTP
CLNDBN Abetalipoproteinaemia
Reversed 0
HGVS NC_000004.11:g.100543913G>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000015311.21,