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rs281875357

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(GC;GC) 0 common in clinvar
Make rs281875357(GC;TG)
Make rs281875357(TG;TG)
ReferenceGRCh38 38.1/141
Chromosome14
Position73219185
GenePSEN1
is asnp
is mentioned by
dbSNPrs281875357
ebirs281875357
HLIrs281875357
Exacrs281875357
Varsomers281875357
Maprs281875357
PheGenIrs281875357
hapmaprs281875357
1000 genomesrs281875357
hgdprs281875357
ensemblrs281875357
gopubmedrs281875357
geneviewrs281875357
scholarrs281875357
googlers281875357
pharmgkbrs281875357
gwascentralrs281875357
openSNPrs281875357
23andMers281875357
23andMe allrs281875357
SNP Nexus

SNPshotrs281875357
SNPdbers281875357
MSV3drs281875357
GWAS Ctlgrs281875357
Max Magnitude0
ClinVar
Risk rs281875357(TG;TG)
Alt rs281875357(TG;TG)
Reference rs281875357(GC;GC)
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.73685893_73685894delGCinsTG
CLNSRC OMIM Allelic Variant
CLNACC RCV000019771.26, RCV000084588.1,