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rs750428882

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs750428882(A;A)
Make rs750428882(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position6616375
GeneTPP1
is asnp
is mentioned by
dbSNPrs750428882
ebirs750428882
HLIrs750428882
Exacrs750428882
Varsomers750428882
Maprs750428882
PheGenIrs750428882
hapmaprs750428882
1000 genomesrs750428882
hgdprs750428882
ensemblrs750428882
gopubmedrs750428882
geneviewrs750428882
scholarrs750428882
googlers750428882
pharmgkbrs750428882
gwascentralrs750428882
openSNPrs750428882
23andMers750428882
23andMe allrs750428882
SNP Nexus

SNPshotrs750428882
SNPdbers750428882
MSV3drs750428882
GWAS Ctlgrs750428882
Max Magnitude0
ClinVar
Risk rs750428882(A;A)
Alt rs750428882(A;A)
Reference rs750428882(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene TPP1
CLNDBN not provided
Reversed 0
HGVS NC_000011.9:g.6637606G>A
CLNSRC
CLNACC RCV000189779.1,