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rs63751122

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;T) 7 Alzheimer's disease
(T;T) 0 common/normal


Make rs63751122(C;C)
ReferenceGRCh38.p7 38.3/150
Chromosome21
Position25891765
GeneAPP
is asnp
is mentioned by
dbSNPrs63751122
dbSNP (classic)rs63751122
ClinGenrs63751122
ebirs63751122
HLIrs63751122
Exacrs63751122
Gnomadrs63751122
Varsomers63751122
LitVarrs63751122
Maprs63751122
PheGenIrs63751122
Biobankrs63751122
1000 genomesrs63751122
hgdprs63751122
ensemblrs63751122
geneviewrs63751122
scholarrs63751122
googlers63751122
pharmgkbrs63751122
gwascentralrs63751122
openSNPrs63751122
23andMers63751122
23andMe allrs63751122
SNPshotrs63751122
SNPdbers63751122
MSV3drs63751122
GWAS Ctlgrs63751122
Max Magnitude7

aka Leu723Pro or L723P

AlzForum


ClinVar
Risk rs63751122(C;C)
Alt rs63751122(C;C)
Reference Rs63751122(T;T)
Significance Untested
Disease not provided
Variation info
Gene APP
CLNDBN not provided
Reversed 1
HGVS NC_000021.8:g.27264077A>G
CLNSRC UniProtKB (protein)
CLNACC RCV000084577.1,