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rs63751287

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs63751287(A;G)
Make rs63751287(G;G)
ReferenceGRCh38 38.1/141
Chromosome14
Position73192792
GenePSEN1
is asnp
is mentioned by
dbSNPrs63751287
ebirs63751287
HLIrs63751287
Exacrs63751287
Varsomers63751287
Maprs63751287
PheGenIrs63751287
hapmaprs63751287
1000 genomesrs63751287
hgdprs63751287
ensemblrs63751287
gopubmedrs63751287
geneviewrs63751287
scholarrs63751287
googlers63751287
pharmgkbrs63751287
gwascentralrs63751287
openSNPrs63751287
23andMers63751287
23andMe allrs63751287
SNP Nexus

SNPshotrs63751287
SNPdbers63751287
MSV3drs63751287
GWAS Ctlgrs63751287
Max Magnitude0
ClinVar
Risk rs63751287(G,T;G,T)
Alt rs63751287(G,T;G,T)
Reference rs63751287(A;A)
Significance Pathogenic
Disease Alzheimer disease not provided
Variation info
Gene PSEN1
CLNDBN Alzheimer disease, type 3 not provided
Reversed 0
HGVS NC_000014.8:g.73659500A>G; NC_000014.8:g.73659500A>T
CLNSRC ClinVar GeneReviews Neurodegenerative Brain Diseases Group
CLNACC RCV000020086.1, RCV000084354.1,