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rs137852703

From SNPedia

Merged intors28936380
Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
(C;G)
(G;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position226885546
GenePSEN2
is asnp
is mentioned by
dbSNPrs137852703
ebirs137852703
HLIrs137852703
Exacrs137852703
Varsomers137852703
Maprs137852703
PheGenIrs137852703
hapmaprs137852703
1000 genomesrs137852703
hgdprs137852703
ensemblrs137852703
gopubmedrs137852703
geneviewrs137852703
scholarrs137852703
googlers137852703
pharmgkbrs137852703
gwascentralrs137852703
openSNPrs137852703
23andMers137852703
23andMe allrs137852703
SNP Nexus

SNPshotrs137852703
SNPdbers137852703
MSV3drs137852703
GWAS Ctlgrs137852703
StatusMerged into rs28936380
Max Magnitude0
OMIM600759
Desc
Variant0007
Relatedalso
ClinVar
Risk rs137852703(G;G)
Alt rs137852703(G;G)
Reference rs137852703(C;C)
Significance Pathogenic
Disease Alzheimer disease
Variation info
Gene PSEN2
CLNDBN Alzheimer disease, type 4
Reversed 0
HGVS NC_000001.10:g.227073247C>G
CLNSRC OMIM Allelic Variant
CLNACC SCV000029617.1,