|
|
| ID |
490 |
| OMIM_ID |
104300
|
| Disease |
Alzheimer disease |
| Gene |
APP
|
| SNP_ID |
rs1787442
|
| 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 |
tctcttcttttctccattttccagtttccc |
| 3'
Near Seq 30 bp |
tgtcctacttagccctttagaaatgcaatt |
| Fasta
Sequence |
aggtgggacc tttgggaggc agttaggatt agattaggtc atgagggcag agcctcacga
tgggactagt gttgaaggga aatgaagaga ccatcttatt cttcaccatg tgaggatgtg
accaagtatc ctcatttttc taagaaaaag agaatgagtt actatttttt tctcttcttt
tctccatttt ccagtttccc
R
tgtcctactt agccctttag aaatgcaatt ataattgttt acctctcctt cacgagacac
tccctacagg gcaaggctgt ctaacatgtg tttcaaagct ccagtgaaac tctccctcac
caggagactg ctcaggagac aacagtcaat ttacaaccca aattatgccc gctacaaaac
tctcccccac ctggagactt
|
|
|
