rs63751163
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;T) | 9 | early-onset Alzheimers disease |
(T;T) | 0 | common in clinvar |
Make rs63751163(C;C) |
Reference | GRCh38 38.1/141 |
Chromosome | 14 |
Position | 73192844 |
Gene | PSEN1 |
is a | snp |
is | mentioned by |
dbSNP | rs63751163 |
dbSNP (classic) | rs63751163 |
ClinGen | rs63751163 |
ebi | rs63751163 |
HLI | rs63751163 |
Exac | rs63751163 |
Gnomad | rs63751163 |
Varsome | rs63751163 |
LitVar | rs63751163 |
Map | rs63751163 |
PheGenI | rs63751163 |
Biobank | rs63751163 |
1000 genomes | rs63751163 |
hgdp | rs63751163 |
ensembl | rs63751163 |
geneview | rs63751163 |
scholar | rs63751163 |
rs63751163 | |
pharmgkb | rs63751163 |
gwascentral | rs63751163 |
openSNP | rs63751163 |
23andMe | rs63751163 |
SNPshot | rs63751163 |
SNPdbe | rs63751163 |
MSV3d | rs63751163 |
GWAS Ctlg | rs63751163 |
Max Magnitude | 9 |
rs63751163, also known as L250S or Leu250Ser, is a SNP in the presenilin 1 PSEN1 gene.
The rare rs63751163(C) allele is considered causative for early-onset Alzheimer's disease.[PMID 9436726]
ClinVar | |
---|---|
Risk | rs63751163(C;C) |
Alt | rs63751163(C;C) |
Reference | Rs63751163(T;T) |
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.73659552T>C |
CLNSRC | OMIM Allelic Variant UniProtKB (protein) |
CLNACC | RCV000019768.27, RCV000084363.1, |