|
|
| ID |
487 |
| OMIM_ID |
104300
|
| Disease |
Alzheimer disease |
| Gene |
APP
|
| SNP_ID |
rs1700992
|
| Organism |
human (Homo sapiens) |
| Variation
Class |
SNP:
single nucleotide polymorphism
|
| Alleles |
A/G
|
| Orientation |
fwd/T |
| Chr-Number |
21 |
| SNP
type |
R |
| Length |
401 |
| 5'
Near Seq 30 bp |
aaaaaatagtaactcattctctttttctta |
| 3'
Near Seq 30 bp |
aaaaatgaggatacttggtcacatcctcac |
| Fasta
Sequence |
Gtctcctgag cagtctcctg gtgagggaga gtttcactgg agctttgaaa acatgttaga
cagccttgcc ctgtagggag tgtctcgtga aggagaggta aacaattata attgcatttc
taaagggcta agtaggacac gggaaactgg aaaatggaga aaagaagaga aaaaaatagt
aactcattct ctttttctta
R
aaaaatgagg atacttggtc acatcctcac atggtgaaga ataagatggt ctcttcattt
cccttcaaca ctagtcccat cgtgaggctc tgccctcatg acctaatcta atcctaactg
cctcccaaag gtcccacctc cacatcccat tattggggat tagggtttca acatagggat
ttgggggaaa cacaaacact
|
|
|
